valeraldehyde
valeric aldehyde
 
Notes:
Found in olive oil and several essential oils. Also present in Bantu beer, plum brandy, cardamom, coriander leaf, rice, Bourbon vanilla, clary sage, cooked shrimps, scallops, apple, banana, sweet cherry, blackcurrant and other foods
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      Let's get reacquainted
      Building great taste with aroma chemicals, extracts, and distillates
      The Alfrebro brand was established in the early 1900s by Alex Fries & Brothers, a Cincinnati Flavor Company. In 1980, the brand was re-launched as an aroma chemical manufacturer. Since its inception, Alfrebro’s primary focus has been to provide quality natural and high value synthetic chemicals.
      Email: Sarah Forbis
      Email: Sales
      Voice: 513-539-3021
      Fax: 513-539-7372
      US Voice: 513-539-7373
      Newsroom
      Product(s):
      n-VALERALDEHYDE NATURAL
       
  • Augustus Oils
    • Augustus Oils Ltd
      The Premier Supplier
      Augustus Oils Ltd, in harmony with nature - to present it at its best...
      A wealth of experience, expertise and knowledge has allowed Augustus to bridge the gulf in expectation and trust between growers and users of natural ingredients. The Company works in partnership with customers on the one hand, and growers, farmers and distillers on the other. Both users and producers can then focus on exactly what they do best, while skilled Augustus technicians closely monitor and control the delivered product. This ensures users can have the confidence that they will receive the best raw materials suited to their requirements.
      Email: Enquiries
      Email: Sales
      Email: web site enquiries
      Voice: +44 (0)1420 590555
      Fax: +44 (0)1420 592420
      Services
      Product(s):
      Aldehyde C5
       
  • 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):
      N-Valeraldehyde
       
  • Indukern F&F
  • 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):
      VALERALDEHYDE
       
  • 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):
      A0425 VALERALDEHYDE
      N0209 NAT. VALERALDEHYDE
       
  • 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
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      22-11500 VALERALDEHYDE
      22-12000 VALERALDEHYDE NATURAL
       
  • Sigma-Aldrich
  • SRS Aromatics
    • SRS Aromatics Ltd
      For over 25 years
      Bringing flavour and fragrance into your world.
      As suppliers / distributors of ingredients to the fragrance and flavour industries, our goal is to provide high quality materials at competitive prices with an exceptional level of service. Established in 1984, SRS Aromatics Ltd is an independent family owned business which has become very well-respected within the fragrance and flavour industry as a reliable and trustworthy partner. Over the years this has allowed the company to develop strong relationships with many global manufacturers; several of whom we represent in the UK. A core aim of our business is to work extremely closely with both our suppliers and customers to maximise service levels with minimum disruption to supply.
      Email: Info
      Email: Sales
      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
      Twitter
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      News
      Product(s):
      VALERALDEHYDE
       
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
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      Product(s):
      V0001 Valeraldehyde >95.0%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 110-62-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 203-784-4
FDA UNII: B975S3014W
Nikkaji Web: J5.096B
Beilstein Number: 1616304
MDL: MFCD00007026
CoE Number: 93
XlogP3-AA: 1.10 (est)
Molecular Weight: 86.13390000
Formula: C5 H10 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: 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: 89  valeraldehyde
DG SANTE Food Flavourings: 05.005  pentanal
FEMA Number: 3098 valeraldehyde
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):110-62-3 ; VALERALDEHYDE
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: colorless to pale yellow clear liquid (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.80500 to 0.80900 @  25.00 °C.
Pounds per Gallon - (est).: 6.698 to  6.732
Refractive Index: 1.39000 to 1.39500 @  20.00 °C.
Melting Point: -92.00 °C. @ 760.00 mm Hg
Boiling Point: 102.00 to  103.00 °C. @ 760.00 mm Hg
Acid Value: 5.00 max. KOH/g
Vapor Pressure: 31.792000 mmHg @ 25.00 °C. (est)
Vapor Density: 3.0 ( Air = 1 )
Flash Point: 55.00 °F. TCC ( 12.78 °C. )
logP (o/w): 1.423 (est)
Soluble in:
 alcohol
 water, 1.17E+04 mg/L @ 25 °C (exp)
Insoluble in:
 water
Similar Items: note
2-oxovaleraldehyde
isovaleraldehyde
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: fermented
 
 fermented  bready  fruity  nutty  berry  
Odor Description:
at 1.00 % in dipropylene glycol. 
fermented bready fruity nutty berry
 
 fermented  bready  fruity  berry  
Odor Description:
Diffusive, fermented, bready, fruity with berry nuances
Mosciano, Gerard P&F 19, No. 2, 55, (1994)
 
 
Flavor Type: winey
 
 winey  fermented  bready  cocoa  chocolate  
Taste Description:
at 25.00 ppm.  
Winey, fermented, bready, cocoa chocolate notes
Mosciano, Gerard P&F 19, No. 2, 55, (1994)
 
Odor and/or flavor descriptions from others (if found).
 
Bedoukian Research
VALERALDEHYDE FCC
Odor Description: In dilution, a coffee, nut-like, chocolate odor
Can be used to lift woody, vanilla-type fragrances.
Taste Description: coffee
An intense topnote for coffee and chocolate flavors.
 
Kingchem Laboratories
VALERALDEHYDE
Odor Description: Very powerful and diffusive, penetrating, acrid-pungent
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
n-VALERALDEHYDE NATURAL
Odor: Woody, Vanilla, Fruity, Nutty
Augustus Oils
Aldehyde C5
Services
Berjé
N-Valeraldehyde
Media
Ernesto Ventós
VALERALDEHYDE BASF
Indukern F&F
VALERIANIC ALDEHYDE
Odor: ALDEHYDIC, POWERFUL, FERMENTED
Kingchem Laboratories
VALERALDEHYDE
Odor: Very powerful and diffusive, penetrating, acrid-pungent
Lluch Essence
VALERALDEHYDE
M&U International
NAT. VALERALDEHYDE
M&U International
VALERALDEHYDE
Nagar Haveli Perfumes & Aromatics
n - Valeraldehyde
Natural
Odor: Fermented bready fruity nutty berry
Penta International
VALERALDEHYDE NATURAL
Penta International
VALERALDEHYDE
Reincke & Fichtner
N-Valeraldehyde
Santa Cruz Biotechnology
For experimental / research use only.
Valeraldehyde
Sigma-Aldrich
Valeraldehyde, ≥97%, FG
Odor: nutty; fruity; vanilla; woody
Certified Food Grade Products
SRS Aromatics
VALERALDEHYDE
TCI AMERICA
For experimental / research use only.
Valeraldehyde >95.0%(GC)
Tengzhou Xiang Yuan Aroma Chemicals
Valeraldehyde
WholeChem
Valeraldehyde
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 11 - Highly flammable.
R 20 - Harmful by inhalation.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 16 - Keep away from sources of ignition - No Smoking.
S 23 - Do not breath vapour.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36/37/39 - Wear suitable clothing, 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-rat LD50  5660 ul/kg
American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969.

oral-mouse LD50  6400 mg/kg
Food and Cosmetics Toxicology. Vol. 17, Pg. 919, 1979.

intraperitoneal-rat LD50  400 mg/kg
BEHAVIORAL: ATAXIA BEHAVIORAL: MUSCLE WEAKNESS
National Technical Information Service. Vol. OTS0533619

intraperitoneal-mouse LD50  200 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ATAXIA BEHAVIORAL: MUSCLE WEAKNESS
National Technical Information Service. Vol. OTS0533619

Dermal Toxicity:
skin-rabbit LD50 5 ml/kg
SKIN AND APPENDAGES (SKIN): "DERMATITIS, OTHER: AFTER SYSTEMIC EXPOSURE"
National Technical Information Service. Vol. OTS0535072

skin-guinea pig LD50 20000 mg/kg
Food and Cosmetics Toxicology. Vol. 17, Pg. 919, 1979.

subcutaneous-mouse LD50 2000 mg/kg
Annales Pharmaceutiques Francaises. Vol. 14, Pg. 710, 1956.

Inhalation Toxicity:
inhalation-rat LCLo 4000 ppm/4H
American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969.

Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: 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
Recommendation for valeraldehyde usage levels up to:
  2.0000 % in the fragrance concentrate.
 
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: 3
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -5.40000
beverages(nonalcoholic): -1.30000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -5.00000
fruit ices: -5.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -4.20000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Authority (EFSA) reference(s):
Flavouring Group Evaluation 3, Revision 1 (FGE.03Rev1): Acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated or unsaturated aldehydes, an ester of a hemiacetal and an orthoester of formic acid, from chemical groups 1, 2 & 4 Commission Regulation (EC) No 1565/2000 of 18 July 2000) [1] - Scientific Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)on a request from the Commission
View page or View pdf
Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species
View page or View pdf
EPI System: View
NIOSH International Chemical Safety Cards: search
NIOSH Pocket Guide: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 110-62-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 8063
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2058
WGK Germany: 1
 pentanal
Chemidplus: 0000110623
EPA/NOAA CAMEO: hazardous materials
RTECS: 110-62-3
Synonyms   Articles   Notes   Search   Top
References:
 pentanal
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 110-62-3
Pubchem (cid): 8063
Pubchem (sid): 134974520
Flavornet: 110-62-3
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
HMDB (The Human Metabolome Database): HMDB31206
FooDB: FDB003228
Export Tariff Code: 2912.19.5000
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
4-methyl-2-(2-methyl propyl)-1,3-oxathiane 
(E)-5-nonen-2-oneFL/FR
alcoholic
 propyl alcoholFL/FR
alliaceous
 methyl furfuryl disulfideFL/FR
amber
 ambrette seed absoluteFL/FR
balsamic
2-acetyl furanFL/FR
 amyl cinnamateFL/FR
isoamyl cinnamateFL/FR
 amyl phenyl acetateFL/FR
 butyl cinnamateFL/FR
 pine needle absoluteFL/FR
berry
 blackberry infusionsFL/FR
 blackberry specialtyFR
 blueberry fragranceFR
 blueberry infusionsFL/FR
 currant fragranceFR
black currant fragranceFR
black currant infusionsFL/FR
 gooseberry fragranceFR
 huckleberry fragranceFR
 mercaptomethyl pentanone 
 methyl beta-ionyl acetateFR
 methyl furoate 
 raspberry essenceFL/FR
black raspberry fragranceFR
 raspberry fragranceFR
 raspberry infusionsFL/FR
 rubus fruticosus fruit extractFL/FR
 rubus idaeus fruit tincture 
bready
 coffee furanoneFL/FR
 furfuralFL/FR
camphoreous
3-benzylidene-2-butanoneFL/FR
beta-homocyclocitralFL/FR
caramellic
 fenugreek oleoresinFL/FR
 maltolFL/FR
 maltyl isobutyrateFL/FR
 shoyu furanoneFL/FR
 toffee furanoneFL/FR
chocolate
isoamyl phenyl acetateFL/FR
 chocolate pyrazine AFL/FR
 cocoa hexenalFL/FR
 cocoa oleoresinFL/FR
 cocoa pentenalFL/FR
2,5-dimethyl pyrazineFL/FR
2,6-dimethyl pyrazineFL/FR
2-methoxypyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
cocoa
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
2-methyl butyraldehydeFL/FR
estery
(E)-tiglyl 2-methyl butyrate 
isopropyl formateFL/FR
 propyl formateFL/FR
fermented
 amyl alcoholFL/FR
 butyl laevo-lactateFL/FR
3-methyl-1-pentanolFL/FR
floral
alpha-damasconeFL/FR
 dihydro-alpha-iononeFL/FR
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
 ethyl phenyl acetateFL/FR
beta-iononeFL/FR
 nerolin fragarolFL/FR
bitter orangeflower concrete moroccoFR
 rose carboxylateFR
fruity
3-benzyl-4-heptanoneFL/FR
 berry hexanoateFR
 berry pentadienoateFL/FR
 blueberry essenceFL/FR
 boysenberry essenceFL/FR
 butyl 2-methyl butyrateFL/FR
 butyl acetoacetateFL/FR
 butyl hexanoateFL/FR
 cherry oxyacetateFL/FR
black currant essenceFL/FR
red currant essenceFL/FR
 cyclohexyl isovalerateFL/FR
 dihydroactinidolideFL/FR
 etaspireneFR
 ethyl (R)-2-hydroxy-4-methyl pentanoateFR
 ethyl (S)-2-hydroxy-4-methyl pentanoateFR
 ethyl 2-hydroxy-3-methyl valerateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 filbert hexenoneFL/FR
 fruit specialtyFR
 geranyl acetoacetateFL/FR
 heliotropyl isobutyrateFL/FR
beta-ionone epoxideFL/FR
 maltyl butyrateFL/FR
 methyl 2-methyl valerateFL/FR
2-methyl butyl 2-methyl butyrateFL/FR
3-nonen-2-oneFL/FR
 osmanthus flower absoluteFL/FR
isopropenyl acetateFL/FR
red raspberry essenceFL/FR
black raspberry essenceFL/FR
 raspberry fruit oilFR
 ribes nigrum fruit extractFL/FR
 ribes rubrum fruit extractFL/FR
isospireneFR
 strawberry glycidate 2FL/FR
 strawberry infusionFL/FR
 styralyl butyrateFL/FR
 vanilla carboxylateFL/FR
 butyl lactateFL/FR
3-cyclohexyl propyl propionate 
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
 phenyl acetaldehydeFL/FR
 thiogeraniolFL/FR
herbal
 barosma betulina leaf oilFL/FR
white cognac oilFL/FR
gamma-valerolactoneFL/FR
mentholic
 menthyl acetate racemicFL/FR
minty
dextro-carvoneFL/FR
musty
2-acetyl pyrroleFL/FR
 cocoa butenalFL/FR
3,6-cocoa pyrazineFL/FR
 filbert pyrazineFL/FR
2,6-lutidineFL/FR
2-methyl pyrazineFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
 vinyl sulfurolFL/FR
popcorn
2-acetyl pyrazineFL/FR
roasted
 fenugreek resinoidFL/FR
 trigonella foenum-graecum seed oil CO2 extractFL/FR
soapy
 ambrettolideFL/FR
spicy
 caraway seed oleoresinFL/FR
 cinnamyl isovalerateFL/FR
black currant bud absoluteFL/FR
(E)-tiglic acidFL/FR
sulfurous
 blackberry thiophenoneFL/FR
 buchu mercaptanFL/FR
(E)-2-octen-1-yl butyrateFL/FR
 phenethyl octanoateFL/FR
woody
 pinacolFR
 
For Flavor
 
No flavor group found for these
 allyl tiglateFL
 amyl phenyl acetateFL/FR
3-benzylidene-2-butanoneFL/FR
 blackberry thiophenoneFL/FR
 butyl acetoacetateFL/FR
 butyl cinnamateFL/FR
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
2(4)-isobutyl-4(2),6-dimethyl dihydro-4H-1,3,5-dithiazineFL
2-butyl-5-ethyl thiopheneFL
 chocolate pyrazine AFL/FR
 chocolate pyrazine BFL
3-cyclohexyl propyl propionate 
 dihydroactinidolideFL/FR
4,5-dimethyl-2-ethyl thiazoleFL
 ethyl 2-hydroxy-3-methyl valerateFL/FR
 geranyl acetoacetateFL/FR
beta-ionone epoxideFL/FR
 menthyl acetate racemicFL/FR
 mercaptomethyl pentanone 
2-methoxypyrazineFL/FR
 methyl furoate 
4-methyl-2-(2-methyl propyl)-1,3-oxathiane 
(E)-5-nonen-2-oneFL/FR
(E)-2-octen-1-yl butyrateFL/FR
(E)-2-octen-4-olFL
 peanut dithiazineFL
 pine needle absoluteFL/FR
 rubus idaeus fruit tincture 
(E)-tiglyl 2-methyl butyrate 
alcoholic
 propyl alcoholFL/FR
balsamic
 amyl cinnamateFL/FR
berry
 blackberry infusionsFL/FR
 blueberry essenceFL/FR
 blueberry infusionsFL/FR
black currant infusionsFL/FR
 dihydro-alpha-iononeFL/FR
 maltyl butyrateFL/FR
 raspberry essenceFL/FR
 raspberry infusionsFL/FR
 rubus fruticosus fruit extractFL/FR
 rubus idaeus fruit extractFL
bitter
 methyl ethoxypyrazineFL
bready
2-propionyl thiazoleFL
brown
 fenugreek oleoresinFL/FR
 furfuralFL/FR
(E)-tiglic acidFL/FR
burnt
 furfuryl alcoholFL
buttery
 butyl laevo-lactateFL/FR
caramellic
 fenugreek resinoidFL/FR
 maltolFL/FR
 shoyu furanoneFL/FR
 toffee furanoneFL/FR
chocolate
 cocoa oleoresinFL/FR
 cocoa propanalFL
 creme de cocoa flavorFL
cocoa
 butyraldehydeFL
 cocoa distillatesFL
 cocoa hexenalFL/FR
coffee
 diisoamyl thiomalateFL
 methyl furfuryl disulfideFL/FR
cooling
beta-homocyclocitralFL/FR
corn chip
2-acetyl-2-thiazolineFL
ethereal
isopropenyl acetateFL/FR
fatty
 cocoa butter distillatesFL
fermented
 methyl thio isovalerateFL
floral
isoamyl cinnamateFL/FR
isoamyl phenyl acetateFL/FR
 cocoa pentenalFL/FR
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
fruity
3-benzyl-4-heptanoneFL/FR
 berry pentadienoateFL/FR
 boysenberry essenceFL/FR
 butyl 2-methyl butyrateFL/FR
 butyl hexanoateFL/FR
 cherry oxyacetateFL/FR
 cinnamyl isovalerateFL/FR
red currant essenceFL/FR
black currant essenceFL/FR
 cyclohexyl isovalerateFL/FR
alpha-damasconeFL/FR
 ethyl (E)-2-methyl-2-pentenoateFL
 ethyl 3-oxohexanoateFL
 ethyl methyl-para-tolyl glycidateFL/FR
 filbert hexenoneFL/FR
 furfuryl isovalerateFL
 heliotropyl isobutyrateFL/FR
 methyl 2-methyl valerateFL/FR
2-methyl butyl 2-methyl butyrateFL/FR
 nerolin fragarolFL/FR
 osmanthus flower absoluteFL/FR
 phenethyl octanoateFL/FR
isopropyl formateFL/FR
 propyl formateFL/FR
red raspberry essenceFL/FR
black raspberry essenceFL/FR
 ribes nigrum fruit extractFL/FR
 ribes rubrum fruit extractFL/FR
 strawberry glycidate 2FL/FR
 strawberry infusionFL/FR
 styralyl butyrateFL/FR
 vanilla carboxylateFL/FR
fusel
 amyl alcoholFL/FR
white cognac oilFL/FR
2-methyl butyraldehydeFL/FR
green
 butyl lactateFL/FR
 cocoa butenalFL/FR
2-ethyl butyraldehydeFL
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
 thiogeraniolFL/FR
herbal
 barosma betulina leaf oilFL/FR
honey
 ethyl phenyl acetateFL/FR
 phenyl acetaldehydeFL/FR
jammy
 maltyl isobutyrateFL/FR
meaty
2,6-dimethyl pyrazineFL/FR
metallic
2,5-dihydroxy-1,4-dithianeFL
minty
dextro-carvoneFL/FR
musty
2,5-dimethyl pyrazineFL/FR
 propionaldehydeFL
2,3,5-trimethyl pyrazineFL/FR
nutty
2-acetyl furanFL/FR
2-acetyl pyrroleFL/FR
3,6-cocoa pyrazineFL/FR
 coffee furanoneFL/FR
2,4-dimethyl-5-vinyl thiazoleFL
 filbert pyrazineFL/FR
2,6-lutidineFL/FR
2-methyl pyrazineFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
 vinyl sulfurolFL/FR
oily
3-nonen-2-oneFL/FR
roasted
2-acetyl pyrazineFL/FR
 trigonella foenum-graecum seed oil CO2 extractFL/FR
soapy
 ambrettolideFL/FR
spicy
 caraway seed oleoresinFL/FR
black currant bud absoluteFL/FR
sulfurous
 buchu mercaptanFL/FR
tonka
gamma-valerolactoneFL/FR
waxy
 furfuryl octanoateFL
whiskey
3-methyl-1-pentanolFL/FR
woody
 ambrette seed absoluteFL/FR
beta-iononeFL/FR
 
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Potential Uses:
 appleFR
 asparagusFL
 bananaFR
 breadFL
 carrotFL
 cedarFR
 celeryFR
 cheeseFL
 chocolate cocoaFL
 clary sage oil replacerFR
 coffeeFR
 cranberryFR
 currantFR
 dry 
 fruitFR
 grapeFR
 guavaFR
 huckleberryFR
 nutFL
 pea green peaFL
 tomatoFL
 vanillaFR
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Occurrence (nature, food, other): note
 allspice plant
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 apple fruit
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 arctic bramble fruit
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 asparagus
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 banana fruit
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 bantu beer
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 barley
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 bay laurel leaf
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 beans
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 beef heated beef
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 beer
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 bilberry fruit fruit
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 brandy
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 brandy grape brandy
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 bread
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 cabbage
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 carrot
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 caviar
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 celery
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 cheeses
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 chicken
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 cider
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 citrus fruits
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 cocoa
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 coffee
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 cranberry fruit
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 currant black currant fruit
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 eucalyptus cinerea
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 eucalyptus dives
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 eucalyptus flobulus
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 eucalyptus hemilampra
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 eucalyptus maideni
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 filbert roasted filbert
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 fish
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 grape
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 guava fruit
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 honey
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 hop oil
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 leek heated leek
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 lovage flower oil @ trace%
Data  GC  Search Trop  Picture
 lovage leaf oil @ trace%
Data  GC  Search Trop  Picture
 meat raw meat
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 milk
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 mint
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 mushroom
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 olive
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 osmanthus absolute @ 0.003%
Data  GC  Search Trop  Picture
 peanut roasted peanut
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 peas
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 pecan roasted pecan
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 plum fruit
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 popcorn
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 pork heated pork
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 potato
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 potato chip
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 potato plant
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 rice plant
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 rose bulgarian
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 rosemary sap
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 rum
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 safflower leaf
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 sage clary sage bulgarian
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 sassafras brazilian
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 sesame seed
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 soybean plant
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 spearmint oil
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 tea
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 tomato
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 trassi cooked trassi
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 turkey
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 walnut black walnut oil
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 walnut english walnut
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 watermelon fruit juice
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 whiskey
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 wine
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Synonyms:
 aldehyde C-5
 amyl aldehyde
 amylaldehyde
 butyl formal
 pentan-1-al
 pentanal
N-pentanal
 pentyl aldehyde
 sucol B
 valeral
N-valeraldehyde
 valeraldehyde FCC
 valeraldehyde, natural
 valerianic aldehyde
 valeric acid aldehyde
 valeric aldehyde
N-valeric aldehyde
 valericaldehyde
 valeryl aldehyde
 valerylaldehyde
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: An Exploration on the Suitability of Airborne Carbonyl Compounds Analysis in relation to Differences in Instrumentation (GC-MS versus HPLC-UV) and Standard Phases (Gas versus Liquid).
J-Stage: Purification and Characterization of Alcohol Dehydrogenase Reducing N-Benzyl-3-Pyrrolidinone from Geotrichum capitatum
PubMed: Recent advances in thermal desorption-gas chromatography-mass spectrometery method to eliminate the matrix effect between air and water samples: Application to the accurate determination of Henry's law constant.
PubMed: Experimental approach to assess sorptive loss properties of volatile organic compounds in the sampling bag system.
PubMed: Functional characterizations of chemosensory proteins of the alfalfa plant bug Adelphocoris lineolatus indicate their involvement in host recognition.
PubMed: Novel approach to test the relative recovery of liquid-phase standard in sorbent-tube analysis of gaseous volatile organic compounds.
PubMed: Rapid analysis of aldehydes by simultaneous microextraction and derivatization followed by GC-MS.
PubMed: Ambient levels of atmospheric carbonyls in Beijing during the 2008 Olympic Games.
PubMed: A combined application of thermal desorber and gas chromatography to the analysis of gaseous carbonyls with the aid of two internal standards.
PubMed: Preparation of furan and thiophene-derived fulvene dialdehydes: synthesis and structural characterization of a 22-oxa-21-carbaporphyrin and a related palladium(II) organometallic complex.
PubMed: Determination of aldehydes in rainwater using micro-solid-phase extraction and high-performance liquid chromatography.
PubMed: Seasonal and diurnal variations of carbonyl compounds in the urban atmosphere of Guangzhou, China.
PubMed: Sorptive removal of odorous carbonyl gases by water.
PubMed: Experimental demonstration of masking phenomena between competing odorants via an air dilution sensory test.
PubMed: Influences of sampling volume and sample concentration on the analysis of atmospheric carbonyls by 2,4-dinitrophenylhydrazine cartridge.
PubMed: Chemical profile of rums as a function of their origin. The use of chemometric techniques for their identification.
PubMed: Purification and characterization of alcohol dehydrogenase reducing N-benzyl-3-pyrrolidinone from Geotrichum capitatum.
PubMed: Enantio- and diastereocontrolled total synthesis of (+)-boronolide.
PubMed: [Determination of major flavor components in chinese spirits using a special domestic gas chromatograph with DNP packed column].
PubMed: [Pollution survey of carbonyl compounds in train air].
PubMed: Determination of aliphatic aldehydes by liquid chromatography with pulsed amperometric detection.
PubMed: Ambient, indoor and personal exposure relationships of volatile organic compounds in Mexico City Metropolitan Area.
PubMed: [Use of chromato-mass-spectrometry for the differential diagnosis of suppurative and nonsuppurative inflammations in the maxillofacial area in children].
PubMed: Stereocontrolled synthesis of (+)-boronolide.
PubMed: Vapor/Solid chemisorption model for passive sampling of aldehydes.
PubMed: Evaluation of n-valeraldehyde modified chitosan as a matrix for hydrophobic interaction chromatography.
PubMed: Time-weighted average sampling of airborne n-valeraldehyde by a solid-phase microextration device.
PubMed: Observation of volatile and semi-volatile carbonyls in an Algerian urban environment using dinitrophenylhydrazine/silica-HPLC and pentafluorophenylhydrazine/silica-GC-MS.
PubMed: Determination of carbonyl compounds in air by electrochromatography.
PubMed: Synthesis of the O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine oximes of selected carbonyl compounds and their determination by liquid chromatography with ultraviolet detection.
PubMed: Airborne aldehydes from heating rosin core solder and liquid rosin flux to soldering temperatures.
PubMed: Optimization of a solid sorbent dynamic personal air sampling method for aldehydes.
PubMed: A new passive sampler for regulated workplace aldehydes.
PubMed: Comparative evaluation of cytotoxicity and metabolism of four aldehydes in two hepatoma cell lines.
PubMed: DNA single and double strand breaks induced by aliphatic and aromatic aldehydes in combination with copper (II).
PubMed: Regulation by progesterone and pregnenolone of dimeric aldehyde dehydrogenase from rat testis cytoplasm.
PubMed: Behavioral responses to food volatiles by two species of stored-product coleoptera,Sitophilus oryzae (curculionidae) andTribolium castaneum (tenebrionidae).
PubMed: Heat sterilization of fluids for peritoneal dialysis gives rise to aldehydes.
PubMed: Catalysis by cytochrome P-450 of an oxidative reaction in xenobiotic aldehyde metabolism: deformylation with olefin formation.
PubMed: Microsomal metabolism of the Z and E isomers of N-nitroso-N-methyl-N-n-pentylamine.
PubMed: Blood and brain n-pentanol in inhalation exposure.
PubMed: DNA-damaging activity of biotic and xenobiotic aldehydes in Chinese hamster ovary cells.
PubMed: Phencyclidine metabolism in vitro. The formation of a carbinolamine and its metabolites by rabbit liver preparations.
PubMed: Efficiency of proton extrusion by chemically modified mitochondria.
PubMed: Effects of aliphatic alcohols and aldehydes on fluidity of spin-labeled synaptosomal plasma membranes.
PubMed: [Synthesis of long chain alkyne and alkene ketoalcohols and their derivatives].
PubMed: The role of (14C, 15N)5-(methylthio) valeraldehyde oxime as a precursor of progoitrin.
PubMed: Attraction of flies by iso-valeraldehyde.
PubMed: Preparation of dihydropyran delta-hydroxyvaleraldehyde and 1,5-pentanediol from tetrahydrofurfuryl alcohol.
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