perillaldehyde
p-mentha-1,8-dien-7-al
 
Notes:
from oil of perillae herba; has neuropharmacological actions. Constit. of Perilla nankinensis and gingergrass oils Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abundantly in the annual herb perilla, but also in a wide variety of other plants and essential oils. It is a monoterpenoid containing an aldehyde functional group.; Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abundantly in the perennial herb perilla, but also in a wide variety of other plants and essential oils. It is a monoterpenoid containing an aldehyde functional group.
  • Beijing Lys Chemicals
    • Beijing Lys Chemicals Co, LTD.
      From Grams to Tons
      Fine chemical high-tech company which contains R&D, production, and sales.
      BEIJING LYS CHEMICALS CO, LTD, established in 2004, is a fine chemical high-tech company which contains R&D, production, and sales. We mainly engaged in export and technology development of flavor and fragrance materials and pharmaceutical intermediates. We have nearly 500 kinds of products, from grams to tons, exported to USA, Europe, South Asia and etc. And we custom manufacture new products according to customers’ needs, and serve good quality products and service. Our goal is to become a fine chemical enterprise which could provide special products and services.
      Email: Mr. Jia
      Email: Mr. Guo
      Voice: 86-10-68418738
      Fax: 86-10-68418739
      Mr. Guo86-10-68483445
      Mr. Guo86-10-68418739
      News
      Product(s):
      10404 Perillaldehyde
       
  • Berjé
    • Berje Inc.
      Where the world comes to its senses
      Where the world comes to its senses - Berjé is a global distributor of Essential Oils and Aromatic Chemicals.
      Berjé is a family-owned business that has been in operation for six decades. The company's origins and strength lie in a profound understanding of the supply and the quality of the diverse raw materials consumed by the flavor and fragrance industries. This base was expanded upon more than two decades ago to include fragrance production. The company's unparalleled raw material expertise is focused on the supply of essential oils and aromatic chemicals. This is supported by our long-standing relationships with a worldwide fabric of producers ensuring the greatest prospects for uninterrupted supply in markets that are often volatile and unpredictable.
      Email: For Information
      Email: For Sales
      Voice: 973-748-8980
      Fax: 973-680-9618
      Instagram
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      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Media
      Products List: View
      Product(s):
      Perilla Aldehyde
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
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      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
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      Product(s):
      2111-75-3 Perillaldehyde 95%
       
  • Fleurchem
    • Fleurchem, Inc.
      Have A Flavorful Day
      A leading global manufacturer and supplier of ingredients for Flavors, Fragrances, AromaTherapy, Foods, Beverages, Personal Care Products, and other uses.
      Operating out of the 200,000 sq. ft., former Hercules/PFW facility in Middletown, NY; Fleurchem produces a full range of natural isolates, synthetic chemicals & specialities, essential oils and flavors. Additionally, the company performs toll manufacturing, as well as custom chemical synthesis for a wide range of clients.
      Email: Information
      US Voice: 845-341-2100
      US Fax: 845-341-2121
      Product(s):
      dihydro cuminyl aldehyde natural
       
  • Foreverest Resources
    • Foreverest Resources Ltd.
      Leading pine based chemicals supplier
      Supplying turpentine based and natural/extracted flavor & fragrance ingredients.
      FOREVERESTA® F&F RAW MATERIALS is a range of natural extracts and synthetic aroma chemicals based on the rich material resources and great supply network from China, which was applied for specialty chemicals industry. The markets cover application areas on food, beverage, custom fragrance, fine perfume, personal care, cosmetics, etc.
      Foreverest Resources Ltd. is a materials supplier, exporting gum turpentine based, terpene derivertives and natural/extracted monomers and intermediates from China since 1988. We offers high quality raw materials for flavors and fragrances synthetic manufacturing in the world.
      Email: Info
      Email: Sales
      Voice: +86 (0)592 5105533
      Fax: +86 (0)592 5151667
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      Product(s):
      Perilla Aldehyde 95%
      Foreverest™ Perilla Aldehyde (Perillaldehyde) is a synthesis of beta-Pinene, appears colorless to pale yellow liquid. It has character with odors of purple perilla, cinnamic aldehyde and cumin aldehyde scent. Perilla Aldehyde can use in formula of fragrance, cosmetics and food.
       
       
  • Indukern F&F
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co., Ltd
      Independent Ingredients Supplier
      We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.
      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
      Email: Info
      Email: Sales
      Voice: 86-510-86023169
      Fax: 86-510-86023170
      Mobile0086-13093133011
      Services
      Biochemical
      Natural Food Colour
      New functional food ingredients
      Product(s):
      HLW-FC043 Perilla aldehyde
       
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Linkedin
      Product(s):
      PERILLA ALDEHYDE
       
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
      Email: Sales
      US Email: Sales
      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
      US Voice: 908-359-9000
      US Fax: 908-359-9002
      News
      Product(s):
      N0324 Nat. Perilla Aldehyde
       
  • Moellhausen
  • O'Laughlin Industries
    • O'Laughlin Industries Inc.
      Manufacturer of chemicals and ingredients used in flavors, fragrances, food, beverages and cosmetics
      Leading the Flavor and Fragrance Industry since 1980.
      O'Laughlin was established in 1980 by its owner and chief executive Michael O'Laughlin, when he moved to Beijing, China and established a small office. Since then it has grown to be a world class producer of chemicals, with significant production facilities in China, and distribution and sales in all major world markets.
      Email: Sales
      US Email: John Gick
      Voice: (852) 2527-1031
      Fax: (852) 2529-0231
      US Voice: (973) 376-4600
      US Fax: (973) 376-4630
      Product(s):
      771-3060 PERILLA ALDEHYDE 90%
      771-3061 PERILLA ALDEHYDE 95%
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
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      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      16-14800 PERILLA ALDEHYDE
      16-14805 PERILLA ALDEHYDE NATURAL
       
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
      US Email: Customer Service
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      Inquiry
      Products List: View
      Product(s):
      W1685 Perilla Aldehyde
       
  • Tianjin Danjun International
    • Tianjin Danjun International Trade Co., LTD.
      Quality Products
      We know the Chinese chemical market well.
      Tianjin danjun international trade co., LTD. is an organic chemicals trading company approved by the relevant state authorities to register. We have about 300 kinds of products (natural aroma chemicals, synthetic aroma chemicals and pharmaceutical intermediates). Most of the products are used in flavor and fragrance industry. We know the Chinese chemical market well and we have close relationship with many of the main manufacturers, and to provide our customers with quality goods together with comprehensive service.
      Email: Info
      Email: Sales
      Voice: +86-15822601686
      Products List: View
      Product(s):
      F-014 Perilla aldehyde
       
  • WholeChem
    • WholeChem, LLC
      Connecting Innovators To the Building Blocks Of the Universe
      Custom manufacturer and distributor of specialty ingredients. We make global local.
      SQF-Certified Supplier
      We owe our success to our integrity, our dedication to the industry, and our commitment to our clients. We invite your inquiries regarding our current product list and any other products you may be having trouble sourcing.
      Email: Info
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      Voice: +1 (262) 995.8668
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      Product(s):
      Perilla aldehyde
       
Synonyms   Articles   Notes   Search
CAS Number: 2111-75-3Picture of molecule3D/inchi
Other(deleted CASRN): 1254961-45-9
ECHA EINECS - REACH Pre-Reg: 218-302-8
FDA UNII: 6EQL0XA86G
Nikkaji Web: J2.142C
MDL: MFCD00001543
CoE Number: 11788
XlogP3-AA: 2.60 (est)
Molecular Weight: 150.22078000
Formula: C10 H14 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic, flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 973  p-mentha-1,8-dien-7-al
DG SANTE Food Flavourings: 05.117  p-mentha-1,8-dien-7-al
FEMA Number: 3557 p-mentha-1,8-dien-7-al
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):2111-75-3 ; PERILLALDEHYDE
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: pale yellow to dark yellow clear oily liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.94000 to 0.95600 @  25.00 °C.
Pounds per Gallon - (est).: 7.822 to  7.955
Refractive Index: 1.50400 to 1.51300 @  20.00 °C.
Optical Rotation: -125.00 to -118.00
Boiling Point: 238.00 to  240.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.043000 mmHg @ 25.00 °C. (est)
Flash Point: 200.00 °F. TCC ( 93.33 °C. )
logP (o/w): 3.053 (est)
Soluble in:
 alcohol
 oils
 water, 160.7 mg/L @ 25 °C (est)
Insoluble in:
 water
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: herbal
 
Odor Strength: high ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 8 hour(s) at 100.00 %
 
 fresh  green  herbal  grassy  sweet  minty  cumin  
Odor Description:
at 10.00 % in dipropylene glycol. 
fresh green herbal grassy sweet mint cumin
Luebke, William tgsc, (1986)
 
 spicy  cumin  cinnamon  pungent  clove  citrus  orange  lime  
Odor Description:
Spicy, cumin, cinnamon, pungent, clove, citrus, orange and lime
Mosciano, Gerard P&F 22, No. 5, 67, (1997)
 
 
Flavor Type: spicy
 
 woody  spicy  waxy  sweet  citrus  lime  aldehydic  
Taste Description:
at 25.00 ppm.  
Woody, spicy, waxy, sweet, citrus, lime and aldehydic
Mosciano, Gerard P&F 22, No. 5, 67, (1997)
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: fragrance
perfuming agents
skin conditioning
Synonyms   Articles   Notes   Search   Top
Suppliers:
Aurochemicals
PERILLA ALDEHYDE (S), Natural
Beijing Lys Chemicals
Perillaldehyde
Berjé
Perilla Aldehyde
Media
BOC Sciences
For experimental / research use only.
Perillaldehyde 95%
Citrus and Allied Essences
laevo-Perilla Aldehyde
Odor: fatty-spicy, oily-herbaceous
Market Report
De Monchy Aromatics
dihydro cuminyl aldehyde
Fleurchem
dihydro cuminyl aldehyde natural
Foreverest Resources
Perilla Aldehyde 95%
Odor: characteristic
Use: Foreverest™ Perilla Aldehyde (Perillaldehyde) is a synthesis of beta-Pinene, appears colorless to pale yellow liquid. It has character with odors of purple perilla, cinnamic aldehyde and cumin aldehyde scent. Perilla Aldehyde can use in formula of fragrance, cosmetics and food.
Indukern F&F
PERILLA ALDEHYDE
Odor: HERBAL, SPICY, CUMIN, SHARP
Inoue Perfumery
PERILLADEHYDE
Jiangyin Healthway
Perilla aldehyde
New functional food ingredients
Lluch Essence
PERILLA ALDEHYDE
M&U International
Nat. Perilla Aldehyde
Moellhausen
PERILLALDEHYDE
Nippon Terpene Chemicals
l-Perillaldehyde 90% up
O'Laughlin Industries
PERILLA ALDEHYDE 90%
O'Laughlin Industries
PERILLA ALDEHYDE 95%
Penta International
PERILLA ALDEHYDE NATURAL
Penta International
PERILLA ALDEHYDE
Reincke & Fichtner
p-Mentha-1,8-dien-7-al
Synerzine
Perilla Aldehyde
Tianjin Danjun International
Perilla aldehyde
WholeChem
Perilla aldehyde
Synonyms   Articles   Notes   Search   Top
Safety Information:
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-mouse LD50  1720 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 799, 1982.

Dermal Toxicity:
skin-guinea pig LD50 > 5000 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 799, 1982.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: cosmetic, flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect: Dermal sensitization
IFRA fragrance material specification:
 Should not be used such that the level in finished cosmetic products exceeds 0.1%. Based on test results showing sensitisation (IFRA guidelines).
IFRA: View Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.054 %
Category 2: Products applied to the axillae
0.016 %
Category 3: Products applied to the face/body using fingertips
0.32 %
Category 4: Products related to fine fragrance
0.30 %
 Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
0.076 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.076 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.076 %
Category 5D: Baby Creams, baby Oils and baby talc
0.076 %
Category 6: Products with oral and lip exposure
0.18 %
 Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.61 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.61 %
Category 8: Products with significant anogenital exposure
0.032 %
Category 9: Products with body and hand exposure, primarily rinse off
0.59 %
 Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
2.10 %
Category 10B: Household aerosol/spray products
2.10 %
 Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
1.20 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
1.20 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
 Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

 
Maximised Survey-derived Daily Intakes (MSDI-EU): 2.10 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 2.00 (μg/capita/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 11
Click here to view publication 11
 average usual ppmaverage maximum ppm
baked goods: -4.50000
beverages(nonalcoholic): -4.00000
beverages(alcoholic): -6.00000
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -6.30000
fruit ices: --
gelatins / puddings: -4.50000
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -20.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: -9.70000
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of alicyclic substances used as flavor ingredients. View pdf
European Food Safety Athority(EFSA): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
List of apha, beta-Unsaturated Aldehydes and Ketones representative of FGE.19 substances for Genotoxicity Testing [1] - Statement of the Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 208 Revision 1 (FGE.208Rev1): Consideration of genotoxicity data on representatives for 10 alicyclic aldehydes with the a,ß-unsaturation in ring / side-chain and precursors from chemical subgroup 2.2 of
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 208 Revision 2 (FGE.208Rev2): Consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 208 Revision 2 (FGE.208Rev2): Consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 208 Revision 3 (FGE.208Rev3): consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 2111-75-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 16441
National Institute of Allergy and Infectious Diseases: Data
SCCNFP: opinion
WGK Germany: 3
 4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
Chemidplus: 0002111753
Synonyms   Articles   Notes   Search   Top
References:
 4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2111-75-3
Pubchem (cid): 16441
Pubchem (sid): 134982357
Flavornet: 2111-75-3
Pherobase: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
CHEBI: View
CHEMBL: View
Golm Metabolome Database: Search
UM BBD: Search
KEGG (GenomeNet): C02576
HMDB (The Human Metabolome Database): HMDB03647
FooDB: FDB014789
Export Tariff Code: 2912.49.0000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 tagete oil rwanda 
aldehydic
 agrumen nitrileFR
 dodecanal (aldehyde C-12 lauric)FL/FR
 fresh carbaldehydeFR
 undecanalFL/FR
alliaceous
 dibutyl sulfideFL/FR
animal
isobutyl quinolineFR
 methyl (E)-2-octenoateFL/FR
anisic
 estragoleFL/FR
 ocimum basilicum leaf oil americaFL/FR
balsamic
 cinnamyl formateFL/FR
 guaiyl acetateFL/FR
christmas pine fragranceFR
camphoreous
2,6-dimethyl-3-oxatricyclo(4.2.1.0*2,4*)nonaneFR
caramellic
2-isobutyl-3-methyl pyrazineFL/FR
cheesy
isovaleric acidFL/FR
chocolate
isobutyl phenyl acetateFL/FR
 cocoa pentenalFL/FR
citrus
isodecyl acetateFR
 lime pyranFR
 litsea cubeba fruit oilFL/FR
 melissa absolute replacerFL/FR
 melissa oil replacerFR
 ocimene quintoxideFL/FR
 verbena absolute franceFL/FR
earthy
 geosminFL/FR
(S)-1-octen-3-olFL/FR
ethereal
 ethyl 4-pentenoateFL/FR
3-decen-2-oneFL/FR
 methyl 2-hexenoateFL/FR
(E)-2-nonenalFL/FR
(E)-2-octenalFL/FR
2-octenalFL/FR
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
floral
 cassis oxime 10%FR
 cilantro herb oil egyptFL/FR
 cymbopogon validus leaf oilFR
 dictamnus hispanicus oilFR
 dihydrocitronellyl ethyl etherFR
 dihydrorose oxideFR
 dimethyl benzyl carbinyl butyrateFL/FR
2,4-dimethyl-3-cyclohexene-1-methanolFR
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
 geranium oil egyptFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 linden flower absoluteFR
 melaleuca ericifolia leaf oilFR
para-methyl benzyl acetateFL/FR
 mimosa absolute franceFL/FR
beta-naphthyl methyl ketoneFL/FR
 neryl formateFL/FR
3-nonanoneFL/FR
isophytolFL/FR
 prenyl salicylateFL/FR
 reseda absoluteFR
 rose butanoateFL/FR
 rose pyranFR
5-tricyclodecenyl acetateFR
 ylang ylang flower oil IFL/FR
fruity
3-butyl bicyclo[3.2.1]-6-octen-2-oneFR
 cinnamyl isobutyrateFL/FR
 ethyl 2-ethyl acetoacetateFL/FR
 ethyl hexanoateFL/FR
1-ethyl-2-methyl propyl chrysanthemumate 
 methyl 2-methyl butyrateFL/FR
2-methyl-2-pentenalFL/FR
 octen-1-yl cyclopentanoneFL/FR
 tropical indeneFR
garlic
4-methyl-2-[2-(methyl thio)ethyl]-1,3-oxathiane 
green
 agrumen aldehydeFR
 bark carbaldehydeFR
 birch leaf specialtyFR
 butyl heptanoateFL/FR
isobutyl heptanoateFL/FR
isobutyl methyl ketoneFL/FR
S-sec-butyl thioisovalerateFL/FR
sec-butyl-3-methyl but-2-ene thioateFL/FR
 carrot leaf oil (daucus carota ssp.maximus)FR
 chrysanthemum carbaldehydeFR
3,7-dimethyl-6-octenoic acidFL/FR
 dodecanal dimethyl acetalFL/FR
 heptanal (aldehyde C-7)FL/FR
 heptanal cyclic propylene acetalFL/FR
3-heptanoneFL/FR
(Z)-3-hepten-1-olFL/FR
3-hepten-2-oneFL/FR
(Z)-4-heptenalFL/FR
2-heptenalFL/FR
 heptyl benzoateFL/FR
2-heptyl furanFL/FR
 heptyl heptanoateFL/FR
 hexanal (aldehyde C-6)FL/FR
 hexanal dihexyl acetalFL/FR
(E)-4-hexen-1-ol 
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexenalFL/FR
3-hexenyl 2-methyl butyrateFL/FR
alpha-hexyl cinnamaldehyde dimethyl acetalFR
english ivy leaf absoluteFR
 lilac acetaldehydeFL/FR
 marigold pot absoluteFL/FR
6-methyl-3-hepten-2-oneFL/FR
(E,Z)-3,6-nonadien-1-olFL/FR
(E,Z)-2,6-nonadienalFL/FR
(E)-2-octen-1-yl acetateFL/FR
3-propyl bicyclo(3.2.1)-6-octen-2-oneFR
 propylene acetalFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
 terpinyl propionateFL/FR
3,5,5-trimethyl hexanolFL/FR
 triplal / ethyl anthranilate schiff's baseFR
9-acetyl-5-methyl-tricyclo[6.2.1.0.sup.2,7 ]undec-4-ene 
 anethum graveolens herb oilFL/FR
 anethum graveolens herb tinctureFL/FR
 anthemis nobilis flower extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
 artemisia alba oilFR
sweet basil absoluteFL/FR
(+)-alpha-campholenic aldehydeFL/FR
 chrysanthemum ketoneFR
 coriander oleoresinFL/FR
2-cyclohexyl cyclohexanoneFR
 dill weed oil cubaFL/FR
 dill weed oil reunionFL/FR
 dimethyl benzyl carbinyl formateFL/FR
2-(2,4-dimethyl-3-cyclohexene-1-yl)-4,4-dimethyl-1,3-oxathianeFR
sweet grass fragranceFR
cis-herbal cyclohexaneFR
 herbal dioxaneFR
 herbal heptaneFR
 hop absoluteFL/FR
 hop oilFL/FR
 lantana camara flower oilFR
 levisticum officinale herb oilFL/FR
 marigold oil mexicoFL/FR
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
1-(2-methyl allyl oxy) heptaneFR
(E)-6-methyl-3-hepten-2-oneFL/FR
 mistletoe absolute 
 monarda fistulosa oilFR
 myrtenolFL/FR
 nonisyl formateFR
(E,Z)-3,5-octadien-2-one 
1-octen-3-yl acetateFL/FR
 oregano specialtyFR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 perilla leaf oilFL/FR
laevo-perillaldehydeFL/FR
 petroselinum crispum seed oil CO2 extractFL/FR
 phenyl acetaldehyde diisoamyl acetalFR
 prenyl senecioateFL/FR
 rosmarinus officinalis extractFL/FR
 rosmarinus officinalis tinctureFL/FR
 tagete oil CO2 extractFL/FR
 theaspiraneFL/FR
 thyme absoluteFL/FR
 thymolFL/FR
 tricyclodecyl acetateFR
 viridiflorolFL/FR
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
honey
 methyl phenyl acetateFL/FR
minty
(-)-menthoneFL/FR
mossy
 treemoss absoluteFR
soapy
 methyl anthranilate / hexyl cinnamaldehyde schiff's baseFR
spicy
 allspice leaf oilFL/FR
isobutyl angelateFL/FR
 cinnamon bark oil (cinnamomum zeylanicum) indiaFL/FR
 cinnamon bark oil ceylonFL/FR
 cinnamon oleoresin ceylonFL/FR
 clove bud oil CO2 extractFL/FR
 croton eluteria bark oilFL/FR
 cuminaldehydeFL/FR
3-(2-furyl) acroleinFL/FR
 ginger root oil chinaFL/FR
 gingergrass oilFR
ortho-methoxycinnamaldehydeFL/FR
 methyl isoeugenolFL/FR
 nutmeg oilFL/FR
 origanum majorana oilFL/FR
 outdoors specialtyFR
black pepper absoluteFL/FR
black pepper oilFL/FR
 pepper tree berry oilFL/FR
 spicy carbonateFR
alpha-phellandreneFL/FR
gamma-terpineneFL/FR
waxy
 ethyl myristateFL/FR
 ethyl octanoateFL/FR
2,4-nonadien-1-olFL/FR
1-undecanolFL/FR
woody
 cinnamyl tiglateFL/FR
 curcuma zedoaria bark extractFL/FR
 dalbergia sissoo leaf oilFR
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
 guaiacyl acetateFL/FR
 sabineneFL/FR
alpha-thujene 
 verdoxanFR
 zedoary bark oilFL/FR
 zedoary root oilFL/FR
 zedoary root oil CO2 extractFL/FR
 
For Flavor
 
No flavor group found for these
4-acetyl-2-isopropenyl pyridineFL
9-acetyl-5-methyl-tricyclo[6.2.1.0.sup.2,7 ]undec-4-ene 
isobutyl heptanoateFL/FR
4-butyl thiazoleFL
S-sec-butyl thioisovalerateFL/FR
sec-butyl-3-methyl but-2-ene thioateFL/FR
 cinnamyl tiglateFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 epoxy-2-decenalFL
 ethyl 4-pentenoateFL/FR
2-ethyl pyridineFL
1-ethyl-2-methyl propyl chrysanthemumate 
 fig leaf absoluteFL
 furfuryl hexanoateFL
3-(2-furyl) acroleinFL/FR
 guaiyl acetateFL/FR
 heptanal cyclic propylene acetalFL/FR
(Z)-3-hepten-1-olFL/FR
2-heptenalFL/FR
2-heptenoic acidFL
 heptyl benzoateFL/FR
(E,E)-2,4-hexadien-1-olFL
 hexanal butane-2,3-diol acetalFL
 hexanal dihexyl acetalFL/FR
 hexanal octane-1,3-diol acetalFL
(Z)-3-hexenoic acidFL
 hexyl (E)-2-hexenoateFL
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
 melissa absolute replacerFL/FR
 melissa oilFL
 methyl 2-hexenoateFL/FR
3-(methyl thio) hexanalFL
4-methyl-2-[2-(methyl thio)ethyl]-1,3-oxathiane 
(E)-6-methyl-3-hepten-2-oneFL/FR
6-methyl-3-hepten-2-oneFL/FR
 mistletoe absolute 
(E,E)-3,5-octadien-2-oneFL
(E,Z)-3,5-octadien-2-one 
(S)-1-octen-3-olFL/FR
2-octenalFL/FR
3-octyl butyrateFL
 perilla leaf oilFL/FR
 prenyl senecioateFL/FR
 propylene acetalFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
 tagete oil rwanda 
alpha-thujene 
ortho-vinyl anisoleFL
 viridiflorolFL/FR
aldehydic
1-undecanolFL/FR
aromatic
laevo-perillaldehydeFL/FR
balsamic
 styrax gum (liquidambar styraciflua)FL
bitter
(E,Z,Z)-2,4,7-tridecatrienalFL/FR
cheesy
isovaleric acidFL/FR
citrus
 lemon carbonylsFL
 lemon lime flavorFL
 litsea cubeba fruit oilFL/FR
 verbena absolute franceFL/FR
cocoa
isobutyl phenyl acetateFL/FR
cooling
 theaspiraneFL/FR
creamy
3-hepten-2-oneFL/FR
earthy
 geosminFL/FR
fatty
2,4-decadienalFL
(E,E)-2,4-heptadienalFL
2-heptyl furanFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
2,4-nonadien-1-olFL/FR
2,4-nonadienalFL
(E)-2-octenalFL/FR
floral
 cocoa pentenalFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
3,7-dimethyl-6-octenoic acidFL/FR
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
 geranium oil egyptFL/FR
 methyl phenyl acetateFL/FR
beta-naphthyl methyl ketoneFL/FR
 ylang ylang flower oil IFL/FR
fruity
 butyl heptanoateFL/FR
 cinnamyl isobutyrateFL/FR
 ethyl 2-ethyl acetoacetateFL/FR
 ethyl hexanoateFL/FR
 lilac acetaldehydeFL/FR
 methyl (E)-2-octenoateFL/FR
 methyl 2-methyl butyrateFL/FR
para-methyl benzyl acetateFL/FR
2-methyl-2-pentenalFL/FR
 neryl formateFL/FR
 octen-1-yl cyclopentanoneFL/FR
 rose butanoateFL/FR
 tagete oil CO2 extractFL/FR
green
 anethum graveolens herb tinctureFL/FR
isobutyl angelateFL/FR
isobutyl methyl ketoneFL/FR
2-isobutyl-3-methyl pyrazineFL/FR
(+)-alpha-campholenic aldehydeFL/FR
 celery distillatesFL
3-decen-2-oneFL/FR
 dibutyl sulfideFL/FR
 dihydroxyacetophenone (mixed isomers)FL
 dodecanal dimethyl acetalFL/FR
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
 heptanal (aldehyde C-7)FL/FR
(Z)-4-heptenalFL/FR
 heptyl heptanoateFL/FR
 hexanal (aldehyde C-6)FL/FR
(E)-4-hexen-1-ol 
(Z)-3-hexenalFL/FR
3-hexenyl 2-methyl butyrateFL/FR
 marigold pot absoluteFL/FR
(E,Z)-3,6-nonadien-1-olFL/FR
(E,Z)-2,6-nonadienalFL/FR
3-nonanoneFL/FR
(E)-2-nonenalFL/FR
 ocimene quintoxideFL/FR
(E,E)-2,4-octadienalFL
(E)-2-octen-1-yl acetateFL/FR
1-octen-3-yl acetateFL/FR
 terpinyl propionateFL/FR
3,5,5-trimethyl hexanolFL/FR
herbal
 anethum graveolens herb oilFL/FR
 anthemis nobilis flower extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
sweet basil absoluteFL/FR
 celery seed oleoresinFL
 cilantro herb oil egyptFL/FR
 coriander oleoresinFL/FR
 dill weed oil cubaFL/FR
 dill weed oil reunionFL/FR
 hop absoluteFL/FR
 hop oilFL/FR
 marigold oil mexicoFL/FR
 ocimum basilicum leaf oil americaFL/FR
 origanum majorana oilFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
 petroselinum crispum seed oil CO2 extractFL/FR
 prenyl salicylateFL/FR
 rosmarinus officinalis extractFL/FR
 rosmarinus officinalis tinctureFL/FR
 thyme absoluteFL/FR
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
ketonic
3-heptanoneFL/FR
licorice
 estragoleFL/FR
minty
(-)-menthoneFL/FR
 myrtenolFL/FR
oily
isophytolFL/FR
phenolic
 thymolFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
spicy
 allspice leaf oilFL/FR
 cinnamon bark oil (cinnamomum zeylanicum) indiaFL/FR
 cinnamon bark oil ceylonFL/FR
 cinnamon oleoresin ceylonFL/FR
 cinnamyl formateFL/FR
 clove bud oil CO2 extractFL/FR
 cola acuminata seed tinctureFL
 croton eluteria bark oilFL/FR
 cuminaldehydeFL/FR
 ginger root oil chinaFL/FR
 levisticum officinale herb oilFL/FR
ortho-methoxycinnamaldehydeFL/FR
 methyl isoeugenolFL/FR
 nutmeg oilFL/FR
black pepper absoluteFL/FR
black pepper oilFL/FR
 pepper tree berry oilFL/FR
terpenic
alpha-phellandreneFL/FR
gamma-terpineneFL/FR
waxy
 ethyl myristateFL/FR
 ethyl octanoateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hydroxycitronellalFL/FR
 mimosa absolute franceFL/FR
 undecanalFL/FR
woody
 curcuma zedoaria bark extractFL/FR
 guaiacyl acetateFL/FR
 sabineneFL/FR
 zedoary bark oilFL/FR
 zedoary root oilFL/FR
 zedoary root oil CO2 extractFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFR
 blackberryFR
 citrusFR
 cumin oil replacerFR
 grapefruitFR
 grass 
 greenFR
 herbalFR
 labdanumFR
 limeFR
 mandarinFR
 mintFR
 orangeFR
 peppermintFR
 spearmintFR
 tea black teaFL
 tea green teaFR
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 amomum testaceum ridl. fruit oil malaysia @ 0.30%
Data  GC  Search Trop  Picture
 blackberry fruit
Search  PMC Picture
 blood orange oil (citrus sinensis l. var. sanguinello) italy @ 0.009%
Data  GC  Search Trop  Picture
 blood orange oil (citrus sinensis l. var. tarocco) italy @ 0.008%
Data  GC  Search Trop  Picture
 blood orange oil italy @ 0.010%
Data  GC  Search Trop  Picture
 caraway seed
Search Trop  Picture
 celery seed
Search Trop  Picture
 costmary oil @ 0.43%
Data  GC  Search Trop  Picture
 cumin seed
Search Trop  Picture
 cumin seed oil turkey @ 2.4%
Data  GC  Search Trop  Picture
 fleabane oil @ 0.10%
Data  GC  Search Trop  Picture
 ginger rhizome oil
Search Trop  Picture
 gingergrass oil @ 0.21%
Data  GC  Search Trop  Picture
 grapefruit juice
Search Trop  Picture
 grapefruit oil
Search Trop  Picture
 grapefruit oil c.p. @ 0.03%
Data  GC  Search Trop  Picture
 grapefruit oil california @ 0.05%
Data  GC  Search Trop  Picture
 grapefruit oil CO2 extract @ 0.05%
Data  GC  Search Trop  Picture
 labdanum siam
Search  PMC Picture
 lemon fruit
Search Trop  Picture
 lemon oil california @ 0.03%
Data  GC  Search Trop  Picture
 lime fruit
Search Trop  Picture
 lime fruit juice
Search Trop  Picture
 lime oil distilled mexico @ 0.02%
Data  GC  Search Trop  Picture
 lime oil distilled peru @ 0.05%
Data  GC  Search Trop  Picture
 lime oil expressed florida @ trace%
Data  GC  Search Trop  Picture
 lime peel oil
Search Trop  Picture
 mandarin fruit
Search Trop  Picture
 mandarin oil @ 0.53%
Data  GC  Search Trop  Picture
 mandarin oil @ trace%
Data  GC  Search Trop  Picture
 mandarin oil italy @ trace%
Data  GC  Search Trop  Picture
 mandarin oil uruguay @ 0.02-0.04%
Data  GC  Search Trop  Picture
 mandarin peel
Search Trop  Picture
 mikan peel oil @ trace%
Data  GC  Search Trop  Picture
 orange fruit
Search Trop  Picture
 orange oil
Search Trop  Picture
 orange oil terpeneless @ 0.80%
Data  GC  Search Trop  Picture
 orange peel oil bitter china @ 0.01%
Data  GC  Search Trop  Picture
 orange peel oil bitter italy @ 0.03%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.009%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.013%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.014%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.015%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. blond italy @ 0.015%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. florida @ 0.01%
Data  GC  Search Trop  Picture
 orange peel oil sweet c.p. valencia @ 0.01%
Data  GC  Search Trop  Picture
 pepper black pepper fruit
Search Trop  Picture
 peppermint
Search Trop  Picture
 spearmint oil
Search Trop  Picture
 tea black tea
Search Trop  Picture
 tsauri grass oil @ 0.90%
Data  GC  Search Trop  Picture
 yuzu peel oil c.p. @ 0.01-0.02%
Data  GC  Search Trop  Picture
 yuzu peel oil CO2 extract @ trace-0.05%
Data  GC  Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
1-cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-
1-cyclohexene-1-carboxaldehyde, 4-isopropenyl-
 dihydro cuminyl aldehyde
 dihydro cuminyl aldehyde natural
 dihydrocuminic aldehyde
 dihydrocuminyl aldehyde
 dihydrocuminylaldehyde
p-mentha-1,8-dien-7-al
para-mentha-1,8-dien-7-al
1,8-p-menthadien-7-al
4-(1-methyl ethenyl)-1-cyclohexene-1-carboxaldehyde
4-(1-methylethenyl)-1-cyclohexene-1-carboxaldehyde
4-(1-methylethenyl)-1-cyclohexene1-carboxyaldehyde
 perilla aldehyde
 perilla aldehyde natural
 perillaaldehyde
 perillal
DL-perillaldehyde
 perillic aldehyde
 perillyl aldehyde
 perillylaldehyde
4-(prop-1-en-2-yl)cyclohex-1-ene-1-carbaldehyde
4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
4-isopropenyl cyclohex-1-ene carbaldehyde
4-isopropenyl-1-cyclohexene-1-carbaldehyde
4-isopropenyl-1-cyclohexene-1-carboxaldehyde
4-isopropenylcyclohex-1-enecarbaldehyde
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Antimicrobial activity of Ammodaucus leucotrichus fruit oil from Algerian Sahara.
PubMed: Fumigant activity of eleven essential oil compounds and their selected binary mixtures against Culex pipiens pallens (Diptera: Culicidae).
PubMed: Two types of alcohol dehydrogenase from Perilla can form citral and perillaldehyde.
PubMed: Synthesis and antiproliferative effects of amino-modified perillyl alcohol derivatives.
PubMed: Chemical composition and mosquito repellency of essential oil of Conyza newii propagated in different geographical locations of Kenya.
PubMed: Effects of perillaldehyde on alternations in serum cytokines and depressive-like behavior in mice after lipopolysaccharide administration.
PubMed: Dominant colonization and inheritance of Methylobacterium sp. strain OR01 on perilla plants.
PubMed: Concise total synthesis of spirocurcasone.
PubMed: Efficient preparation of Hangekobokuto (Banxia-Houpo-Tang) decoction by adding perilla herb before decoction is finished.
PubMed: Whole-cell-based CYP153A6-catalyzed (S)-limonene hydroxylation efficiency depends on host background and profits from monoterpene uptake via AlkL.
PubMed: Enhancing antioxidant capacity and reducing decay of chinese bayberries by essential oils.
PubMed: Influence of the active compounds of Perilla frutescens leaves on lipid membranes.
PubMed: Antibacterial activity of the essential oil and main components of two Dracocephalum species from Iran.
PubMed: Development of quality assessment method for optically active food flavor chemicals.
PubMed: Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.
PubMed: (S)-Perillaldehyde azine.
PubMed: Inhibitory activity of hydrosols, herbal teas and related essential oils against filament formation and the growth of Candida albicans.
PubMed: Chemical composition and antimicrobial activity of the extracts of Kefe cumin (Laser trilobum L.) fruits from different regions.
PubMed: Preliminary analysis on essential oil composition of Perilla L. cultivated in Lithuania.
PubMed: A nine-step total synthesis of (-)-platencin.
PubMed: Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants.
PubMed: Taste-guided identification of high potency TRPA1 agonists from Perilla frutescens.
PubMed: Fragrant unsaturated aldehydes elicit activation of the Keap1/Nrf2 system leading to the upregulation of thioredoxin expression and protection against oxidative stress.
PubMed: Antidepressant-like Effect of l-perillaldehyde in Stress-induced Depression-like Model Mice through Regulation of the Olfactory Nervous System.
PubMed: Conformational flexibility in terpenes: vibrational circular dichroism (VCD), infrared and Raman study of S-(-)-perillaldehyde.
PubMed: The monoterpenoids citral and geraniol are moderate inhibitors of CYP2B6 hydroxylase activity.
PubMed: Opposite stereochemical courses for enzyme-mediated alkene reductions of an enantiomeric substrate pair.
PubMed: Increasing antioxidant activity and reducing decay of blueberries by essential oils.
PubMed: Influence of cinnamon and clove essential oils on the D- and z-values of Escherichia coli O157:H7 in apple cider.
PubMed: Parectadial, a monoterpenoid from the defensive spray of Parectatosoma mocquerysi.
PubMed: Synthesis and biological activity of novel pyranopyrones derived from engineered aromatic polyketides.
PubMed: Biotransformation of terpenoids by mammals, microorganisms, and plant-cultured cells.
PubMed: Antimicrobial effect of trans-cinnamaldehyde, (-)-perillaldehyde, (-)-citronellal, citral, eugenol and carvacrol on airborne microbes using an airwasher.
PubMed: Analysis by gas chromatography-mass spectrometry of the volatiles from the fruits of Ammodaucus leucotrichus subsp. leucotrichus and subsp. nanocarpus grown in North Africa and the Canary Islands, respectively.
PubMed: Vasodilative effect of perillaldehyde on isolated rat aorta.
PubMed: Fumigant toxicity of the essential oils of some African plants against Anopheles gambiae sensu stricto.
PubMed: Repellency of essential oils of some Kenyan plants against Anopheles gambiae.
PubMed: Antibacterial activities of naturally occurring compounds against antibiotic-resistant Bacillus cereus vegetative cells and spores, Escherichia coli, and Staphylococcus aureus.
PubMed: Essential oils: their antibacterial properties and potential applications in foods--a review.
PubMed: Study of the carbonyl products of terpene/OH radical reactions: detection of the 2,4-DNPH derivatives by HPLC-MS.
PubMed: Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae.
PubMed: Perillyl alcohol and perillaldehyde induced cell cycle arrest and cell death in BroTo and A549 cells cultured in vitro.
PubMed: Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, Rhizoglyphus sp.
PubMed: Bactericidal activities of plant essential oils and some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.
PubMed: Carvone and perillaldehyde interfere with the serum-induced formation of filamentous structures in Candida albicans at substantially lower concentrations than those causing significant inhibition of growth.
PubMed: Cytotoxicity and biotransformation of the anticancer drug perillyl alcohol in PC12 cells and in the rat.
PubMed: Effects of branched cyclodextrins on the solubility and stability of terpenes.
PubMed: Quantification of carvone, cineole, perillaldehyde, perillyl alcohol and sobrerol by isocratic high-performance liquid chromatography.
PubMed: Insecticidal activity of monoterpenoids to western corn rootworm (Coleoptera: Chrysomelidae), twospotted spider mite (Acari: Tetranychidae), and house fly (Diptera: Muscidae).
PubMed: Isoprenoids suppress the growth of murine B16 melanomas in vitro and in vivo.
PubMed: cDNA cloning, characterization, and functional expression of 4S-(-)-limonene synthase from Perilla frutescens.
PubMed: Genetic analysis of essential oil variants in Perilla frutescens.
PubMed: Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.
PubMed: [Constituents of essential oils from leaves, stems, and fruits of Perilla frutescens (L.) Britt].
PubMed: Olfactory sensitivity of two sympatric species of rice leaf folders (Lepidoptera: Pyralidae) to plant volatiles.
PubMed: Hepatic microsomal oxygenation of aldehydes to carboxylic acids.
PubMed: Terpenoid biotransformation in mammals. V. Metabolism of (+)-citronellal, (+-)-7-hydroxycitronellal, citral, (-)-perillaldehyde, (-)-myrtenal, cuminaldehyde, thujone, and (+-)-carvone in rabbits.
PubMed: [Pharmacological studies on Perillae Herba. I. Neuropharmacological action of water extract and perillaldehyde (author's transl)].
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