dextro-camphor
D-camphor
 
Notes:
None found
  • 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
      Linkedin
      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Media
      Products List: View
      Product(s):
      Camphor Gum Synthetic
      Camphor Gum Natural
       
  • 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
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-485-4226
      Fax: 1-631-614-7828
      US Voice: 1-631-485-4226
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
      Facebook
      Twitter
      Linkedin
      Blog
      Get the App!
      Product(s):
      464-49-3 D(+)-Camphor =>98%
       
  • ECSA Chemicals
    • ECSA Chemicals
      Human Chemistry
      ECSA Chemicals has been active since 1913 in the trading and international commerce of raw materials. With an organisation divided into industrial segments managed by specialists, it has become one of the largest distributors worldwide.
      ECSA Chemicals is the largest Swiss-owned company in terms of warehouses for the distribution of chemical products. We have been distributing chemical products for over 100 years and we have a special interest in protecting the environment and in the safety of our facilities and collaborators.
      Established in 1913 as a small grocery store, in its over 100 years of activity ECSA Chemicals has become one of the most important Swiss-owned distributors of chemical products. The company, which is active in international distribution and trading, is organised into industrial segments that are managed by teams of specialists and experts. They guarantee professional and customised consultancy and services. With our experience, we can rapidly and safely connect you with the best suppliers on the market, providing you with a complete search, consulting and assistance service. The focus of our approach and operations is you, our customers. We strive every day to find the best products that satisfy your needs as quickly as possible. Your satisfaction is our greatest success. WHY CHOOSE ECSA? EXPERIENCE We have been working for 100 years. QUALITY We have obtained many certifications (ISO, SQAS, GDP, Responsible Care, Bio-Inspecta, RSPO, etc.). We guarantee full compliance with the current laws and continuous training for our staff. SAFETY We constantly carry out risk analyses for each infrastructure, defining safety levels and implementing corrective measures promptly wherever they are needed. WIDESPREAD DISTRIBUTION We have warehouses in strategic locations to supply goods to Switzerland and to the rest of the world. STORAGE CAPACITY The 3 ECSA-owned warehouses guarantee considerable storage area and capacity in each warehouse, with full availability of products (base chemicals and speciality chemicals). SPEED Presence all over the country, staff dedicated to sourcing raw materials and considerable storage capacity guarantee that goods are rapidly obtained and supplied. CONSULTANCY Our specialists - in-depth knowledge of the market and products allows us to provide full consulting services, from the purchase to the supply of raw materials.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
      Linkedin
      Youtube
      RSS Feed
      ECSA Trade
      ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
      Products List: View
      Product(s):
      MP-018465 CAMPHOR NATURAL
       
  • Excellentia International
    • Excellentia International
      Ingredients by Nature
      Exceptional quality and excellence in meeting our customers requirements.
      Excellentia International was founded in 2010 through the merger of Excellentia Flavors LLC and Polarome International. Collectively, these companies account for more than one hundred years of industry experience, and are recognized for exceptional quality and excellence in meeting our customers’ requirements.
      Email: Info
      Email: Sales
      Email: Regulatory
      Voice: 732.749.9840
      Our Services
      Product(s):
      Camphor, d- Natural
       
  • 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):
      camphor (gum) powder USP
      camphor (gum) powder, technical
       
  • 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):
      CAMPHOR POWDER NATURAL
       
  • 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):
      A0018 Camphor Powder, Kosher
      N0323 Nat. Camphor
       
  • Moellhausen
  • 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):
      03-04700 D-CAMPHOR USP NATURAL
      03-04702 D-CAMPHOR CRYSTALS
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
      Email: Enquiries
      Email: Sales
      Voice: +66(0)2-99-800-80
      Fax: +66(0)2-99-800-80
      PerfumersWorld Skype Skype
      Facebook
      Twitter
      Google+
      Youtube
      Resources
      Software: Perfumer's Workbook
      Product(s):
      1BH00080 Camphor Powder
       
  • Prodasynth
    • Prodasynth
      PRODUCTEUR PAR ESSENCE
      Chemical specialist in manufacturing, distributing and sourcing of tailor-made ingredients for the Flavour & Fragrance industry.
      Today we are also proud to say, we have created an important range of Natural Molecules which can be found in our Raw Material Compendium. The versatility of our small but efficient structure is one of our main strengths when trying to fulfill our clients' requirements.
      Email: Info:
      Email: Sales Team Prodasynth
      Voice: (33) 4 93 09 00 11
      Fax: (33) 4 22 13 07 38
      New Catalog
      Products List: View
      Product(s):
      CAMPHOR-D, NATURAL (> 96%)
       
  • 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
      Linkedin
      News
      Product(s):
      CAMPHOR POWDER DEXTRO
       
  • 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
      Twitter
      Instagram
      Linkedin
      Product(s):
      C0010 (+)-Camphor >98.0%(GC)
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
      Email: Enquiries
      US Email: Enquiries
      Voice: +44 (0) 1284 702500
      Fax: +44 (0) 1284 703809
      US Voice: +1 863 668 9500
      US Fax: +1 863 668 3388
      Twitter
      Linkedin
      Youtube
      News
      Product(s):
      Camphor Powder
       
  • Ernesto Ventós
  • 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
      Email: Orders
      Voice: +1 (262) 995.8668
      Certification
      Our Services
      Products List: View
      Product(s):
      D-Camphor, Natural
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 464-49-3Picture of molecule3D/inchi
Other(deleted CASRN): 68546-28-1
ECHA EINECS - REACH Pre-Reg: 207-355-2
FDA UNII: N20HL7Q941
Nikkaji Web: J43.294F
Beilstein Number: 2042745
MDL: MFCD00064149
CoE Number: 140
XlogP3-AA: 2.20 (est)
Molecular Weight: 152.23672000
Formula: C10 H16 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
EFSA/JECFA Comments: JECFA evaluated d-camphor (CASrn as in Register). CASrn in Register refers to (1R,4R)-1,7,7-Trimethylbicyclo(2.2.1)-heptan-2-one (d-camphor).
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: 1395  D-camphor
DG SANTE Food Flavourings: 07.215  D-camphor
FEMA Number: 2230 D-camphor
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):464-49-3 ; D-CAMPHOR
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.


FDA PART 175 -- INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS
Subpart B--Substances for Use Only as Components of Adhesives
Sec. 175.105 Adhesives.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: white colorless crystals (est)
Assay: 97.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 178.80 °C. @ 760.00 mm Hg
Boiling Point: 207.40 °C. @ 760.00 mm Hg
Vapor Pressure: 4.000000 mmHg @ 25.00 °C.
Vapor Density: 5.24 ( Air = 1 )
Flash Point: 148.00 °F. TCC ( 64.44 °C. )
logP (o/w): 3.040
Soluble in:
 alcohol
 water, 100 mg/L @ 25 °C (exp)
Insoluble in:
 water
 glycerin
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: camphoreous
 
Odor Strength: high ,
recommend smelling in a 10.00 % solution or less
 
Substantivity: 160 hour(s) at 20.00 % in dipropylene glycol
 
 camphoreous  minty  phenolic  herbal  woody  
Odor Description:
at 10.00 % in dipropylene glycol. 
camphor minty phenolic herbal woody
Luebke, William tgsc, (1988)
 
 camphoreous  medicinal  mentholic  cooling  green  
Odor Description:
Camphoreous, medicinal, mentholic, with a cooling green nuance
Mosciano, Gerard P&F 18, No. 2, 38, (1993)
 
 
Flavor Type: medicinal
 
 medicinal  camphoreous  mentholic  woody  
Taste Description:
at 20.00 ppm.  
Medicinal, camphoreous, mentholic and woody
Mosciano, Gerard P&F 18, No. 2, 38, (1993)
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfa Biotechnology
For experimental / research use only.
D-camphre 98%
Berjé
Camphor Gum Natural
Media
Berjé
Camphor Gum Synthetic
BOC Sciences
For experimental / research use only.
D(+)-Camphor =>98%
Diffusions Aromatiques
CAMPHRE-D NATUREL
ECSA Chemicals
CAMPHOR NATURAL
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
Ernesto Ventós
CAMPHOR-D NATURAL
Excellentia International
Camphor, d- Natural
ExtraSynthese
For experimental / research use only.
(+)-Camphor (GC) ≥97% (sum of enantiomers)
Fleurchem
camphor (gum) powder USP
Fleurchem
camphor (gum) powder, technical
Indukern F&F
CAMPHOR POWDER NATURAL
Odor: AROMATIC, FRESH, CONIFEROUS
Lluch Essence
CAMPHOR POWDER NATURAL
M&U International
Camphor Powder, Kosher
M&U International
Nat. Camphor
Moellhausen
CAMPHOR NAT.
Penta International
D-CAMPHOR CRYSTALS
Penta International
D-CAMPHOR USP NATURAL
PerfumersWorld
Camphor Powder
Odor: camphor conifer fresh-woody cool
Phoenix Aromas & Essential Oils
Camphor Natural
Prodasynth
CAMPHOR-D, NATURAL
(> 96%)
R C Treatt & Co Ltd
Camphor Powder
Reincke & Fichtner
D-Camphor natural
Reincke & Fichtner
D-Camphor
Sigma-Aldrich
D-Camphor, ≥97%, FG
Odor: medicinal; woody; vanilla
Certified Food Grade Products
Sigma-Aldrich
D-Camphor, natural, 96%, FG
SRS Aromatics
CAMPHOR POWDER DEXTRO
Odor: Camphor, Minty, Phenolic, Herbal, Woody
TCI AMERICA
For experimental / research use only.
(+)-Camphor >98.0%(GC)
Vistachem
Camphor, natural
WholeChem
D-Camphor, Natural
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 10 - Flammable.
R 20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
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 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
 
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  1310 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

intraperitoneal-cat LDLo  400 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

intravenous-mouse LD90  525 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

intraperitoneal-rat LDLo  3500 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

Dermal Toxicity:
subcutaneous-mouse LDLo 2200 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

subcutaneous-rat LDLo 1700 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 665, 1978.

Inhalation Toxicity:
Not determined
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 dextro-camphor usage levels up to:
  3.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 50.00 (μg/capita/day)
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: -11.00000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: -20.00000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.10000
fruit ices: -0.10000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: 1.1000025.00000
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:
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):
Camphor in flavourings and other food ingredients with flavouring properties - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food on a request from the Commission
View page or View pdf
Safety and efficacy of secondary alicyclic saturated and unsaturated alcohols, ketones, ketals and esters with ketals containing alicyclic alcohols or ketones and esters containing secondary alicyclic alcohols from chemical group 8 when used as flavourings for all animal species
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 464-49-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 159055
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 2717
WGK Germany: 1
 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Chemidplus: 0000464493
EPA/NOAA CAMEO: hazardous materials
RTECS: EX1260000 for cas# 464-49-3
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: Chirality or Article
 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 464-49-3
Pubchem (cid): 159055
Pubchem (sid): 134973831
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
FDA Indirect Additives used in Food Contact Substances:View
CHEBI: View
CHEMBL: View
UM BBD: Search
KEGG (GenomeNet): C00808
HMDB (The Human Metabolome Database): Search
FooDB: FDB009067
Export Tariff Code: 2914.21.1000
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
aldehydic
aldehydic
 decanal (aldehyde C-10)FL/FR
 dodecanal (aldehyde C-12 lauric)FL/FR
 nonanal (aldehyde C-9)FL/FR
10-undecenal (aldehyde C-11 undecylenic)FL/FR
amber
 angelica archangelica root oil CO2 extractFL/FR
 cistus ladaniferus resinoidFL/FR
animal
1-oxaspiro-4,7-dodecaneFR
anise
 anise seed oilFL/FR
star anise seed oil chinaFL/FR
 anise seed oil colombiaFL/FR
star anise seed oil spainFL/FR
balsamic
isoamyl benzoateFL/FR
 amyris wood oilFL/FR
 benzoinFL/FR
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
dextro,laevo-isoborneolFL/FR
isobornyl acetateFL/FR
 bornyl acetateFL/FR
isobornyl formateFL/FR
isobornyl propionateFL/FR
 cedar forest fragranceFR
 conifer acetateFR
 fir balsam absoluteFR
 frankincense absoluteFL/FR
3-phenyl propyl alcoholFL/FR
camphoreous
 cyclohexanolFL/FR
 melaleuca viridiflora leaf oilFR
citrus
 methyl heptenoneFL/FR
 neroli ketoneFR
creamy
 veratraldehydeFL/FR
earthy
2-octanoneFL/FR
fatty
 decanolFL/FR
floral
 aglaia odorata absoluteFR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
 bigarade oxideFR
isobutyl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 ho leaf oilFR
 karo karounde absoluteFR
 karo karounde absolute replacerFR
 lavender oilFL/FR
 nonanolFL/FR
 petitgrain bigarade oilFL/FR
 phenethyl alcoholFL/FR
 sambucus nigra flower oil CO2 extractFR
5-tricyclodecenyl acetateFR
fruity
 allyl cyclohexyl propionateFL/FR
3-benzyl-4-heptanoneFL/FR
green
isocyclocitral (IFF)FL/FR
 dicyclopentadiene propionateFR
alpha-hexyl cinnamaldehyde dimethyl acetalFR
para-methyl hydratropaldehydeFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
hay
 tobacco leaf absoluteFL/FR
herbal
 ajowan seed oilFL/FR
1-allyl-2,2,7,7-tetramethyl cycloheptanolFR
 angelica archangelica seed extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 artemisia vestita wall. leaf oilFR
 bornyl 2-methyl butyrateFL/FR
 bornyl butyrateFL/FR
beta-bourboneneFL/FR
3-butyl phthalideFL/FR
delta-cadinene 
 calamintha clinopodium oilFR
 cardamom liquid resinFR
 carum carvi fruit oilFL/FR
1,8-cineoleFL/FR
 dill seed oilFL/FR
 dill seed oil CO2 extractFL/FR
 eucalyptus globulus oilFL/FR
 eucalyptus oil replacerFR
 herbal undecanoneFR
 immortelle flower oilFL/FR
abrialis lavandin oilFL/FR
 lavandin water absoluteFL/FR
spike lavender oilFL/FR
2-methyl butyl salicylateFL/FR
 origanum oil greeceFL/FR
alpha-pineneFL/FR
 pinocarveolFL/FR
 piperitoneFL/FR
 rosemary oil spainFL/FR
 rosemary oleoresinFL/FR
 safranalFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
red thyme oil indiaFL/FR
red thyme oil spainFL/FR
 thyme oil wild or creepingFL/FR
 thymolFL/FR
mentholic
 peppermint cyclohexanoneFL/FR
minty
 mint fragranceFR
 mint specialtyFR
 pennyroyal oilFL/FR
mossy
 veramoss (IFF)FR
musk
 angelica root absoluteFL/FR
naphthyl
1-methyl naphthaleneFL/FR
nutty
 pentanoic acid, 3-methyl-2-oxo-, ethyl esterFL/FR
orris
para-isopropyl acetophenoneFL/FR
powdery
para-anisyl alcoholFL/FR
spicy
 bayberry fragranceFR
 cardamom oil replacerFR
 cassia bark oil chinaFL/FR
 cinnamon acroleinFL/FR
 clove bud oilFL/FR
 clove leaf oilFL/FR
 elettaria cardamomum seed oilFL/FR
 elettaria cardamomum seed oil guatemalaFL/FR
 ginger oleoresin africaFL/FR
 ginger root absoluteFL/FR
 ginger root oil cochinFL/FR
 maja fragranceFR
 myrceneFR
2-octanolFL/FR
black pepper absoluteFL/FR
black pepper oilFL/FR
white pepper oilFL/FR
black pepper oleoresinFL/FR
4-isopropyl-2-cyclohexenoneFL/FR
terpenic
 cypress leaf oilFR
 frankincense oilFL/FR
 juniperus communis fruit oilFL/FR
thujonic
 cedarleaf oil western redFR
 sage oil dalmatianFL/FR
common tansy flower oil argentinaFL/FR
common tansy leaf oil dutchFR
 woody ketoneFL/FR
tonka
 tonka bean absoluteFR
waxy
 ethyl laurateFL/FR
woody
 angelica archangelica root extractFL/FR
 angelica archangelica root tinctureFL/FR
 angelica archangelica root waterFL/FR
 cadineneFL/FR
(+)-campheneFL/FR
 campheneFL/FR
 cypress essenceFR
 dalbergia sissoo leaf oilFR
 dihydro-alpha-terpinyl acetateFR
 fougere woody fragranceFR
(1R,4S)-1-hydroxy-1,4-dimethyl spiro(4.6)undecan-2-one 
 laitoneFR
 manevoro oilFR
 marine formateFR
 melaleuca bracteata leaf oilFR
 methyl cedryl ketoneFL/FR
gamma-muurolene 
 origanum vulgare ssp. vulgare oil himalaya 
 patchouli ethanoneFR
 patchouli oilFL/FR
 polylimoneneFL/FR
 santol pentenolFR
 spruce needle oil canadaFL/FR
 tetrahydromugolFR
 thuja occidentalis leaf oilFL/FR
 vetiver oil haitiFL/FR
 woody acetateFR
 
For Flavor
 
No flavor group found for these
 angelica archangelica root extractFL/FR
 angelica archangelica root oil CO2 extractFL/FR
 angelica archangelica root tinctureFL/FR
 angelica archangelica root waterFL/FR
 benzoinFL/FR
 bornyl 2-methyl butyrateFL/FR
 bornyl butyrateFL/FR
beta-bourboneneFL/FR
3-butyl phthalideFL/FR
delta-cadinene 
(+)-campheneFL/FR
 cistus ladaniferus resinoidFL/FR
 cyclohexanolFL/FR
(1R,4S)-1-hydroxy-1,4-dimethyl spiro(4.6)undecan-2-one 
2-methyl butyl salicylateFL/FR
3-methyl cyclohexanoneFL
1-methyl pyrroleFL
gamma-muurolene 
 origanum vulgare ssp. vulgare oil himalaya 
 polylimoneneFL/FR
4-isopropyl-2-cyclohexenoneFL/FR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
 woody ketoneFL/FR
aldehydic
 nonanal (aldehyde C-9)FL/FR
anise
 anise seed oilFL/FR
star anise seed oil chinaFL/FR
 anise seed oil colombiaFL/FR
star anise seed oil spainFL/FR
balsamic
siam benzoin resinoidFL/FR
 benzyl benzoateFL/FR
 benzyl salicylateFL/FR
isobornyl propionateFL/FR
camphoreous
dextro,laevo-isoborneolFL/FR
 bornyl acetateFL/FR
 campheneFL/FR
 pinocarveolFL/FR
citrus
 petitgrain bigarade oilFL/FR
cooling
isobutyl salicylateFL/FR
spike lavender oilFL/FR
creamy
 veratraldehydeFL/FR
dairy
2-octanoneFL/FR
fatty
10-undecenal (aldehyde C-11 undecylenic)FL/FR
floral
 phenethyl alcoholFL/FR
fruity
 allyl cyclohexyl propionateFL/FR
isoamyl benzoateFL/FR
para-anisyl alcoholFL/FR
3-benzyl-4-heptanoneFL/FR
grassy
 tobacco leaf absoluteFL/FR
green
isoamyl salicylateFL/FR
isocyclocitral (IFF)FL/FR
 methyl heptenoneFL/FR
para-methyl hydratropaldehydeFL/FR
herbal
 ajowan seed oilFL/FR
 angelica archangelica seed extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 cardamom distillatesFL
 cardamom flavorFL
 carum carvi fruit oilFL/FR
 celery seed oleoresinFL
 dill seed oilFL/FR
 dill seed oil CO2 extractFL/FR
 eucalyptus flavorFL
 eucalyptus globulus oilFL/FR
 immortelle flower oilFL/FR
abrialis lavandin oilFL/FR
 lavandin water absoluteFL/FR
 lavender oilFL/FR
 origanum oil greeceFL/FR
 rosemary oil spainFL/FR
 rosemary oleoresinFL/FR
white thyme oilFL/FR
 thyme oil (thymus zygis gracillis) spainFL/FR
red thyme oil indiaFL/FR
red thyme oil spainFL/FR
 thyme oil wild or creepingFL/FR
medicinal
 frankincense absoluteFL/FR
mentholic
 peppermint cyclohexanoneFL/FR
minty
1,8-cineoleFL/FR
 pennyroyal oilFL/FR
 piperitoneFL/FR
musk
 angelica root absoluteFL/FR
naphthyl
1-methyl naphthaleneFL/FR
nutty
 pentanoic acid, 3-methyl-2-oxo-, ethyl esterFL/FR
phenolic
 thymolFL/FR
pine
 spruce beer flavorFL
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
spicy
 cassia bark oil chinaFL/FR
 cinnamon acroleinFL/FR
 clove bud oilFL/FR
 clove leaf oilFL/FR
 elettaria cardamomum seed oilFL/FR
 elettaria cardamomum seed oil guatemalaFL/FR
 ginger oleoresin africaFL/FR
 ginger root absoluteFL/FR
 ginger root oil cochinFL/FR
2-octanolFL/FR
black pepper absoluteFL/FR
black pepper oilFL/FR
white pepper oilFL/FR
black pepper oleoresinFL/FR
3-phenyl propyl alcoholFL/FR
para-isopropyl acetophenoneFL/FR
terpenic
 juniperus communis fruit oilFL/FR
thujonic
 sage oil dalmatianFL/FR
common tansy flower oil argentinaFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
waxy
 decanal (aldehyde C-10)FL/FR
 decanolFL/FR
 ethyl laurateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 nonanolFL/FR
woody
 amyris wood oilFL/FR
isobornyl acetateFL/FR
isobornyl formateFL/FR
 cadineneFL/FR
 frankincense oilFL/FR
 methyl cedryl ketoneFL/FR
 patchouli oilFL/FR
alpha-pineneFL/FR
 safranalFL/FR
 spruce needle oil canadaFL/FR
 thuja occidentalis leaf oilFL/FR
 vetiver oil haitiFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 basil oil replacerFR
 camphor tree barkFL/FR
 cologneFR
 disinfectants 
 floralFR
 lavandinFR
 lavenderFR
 lavender spike lavenderFL/FR
 nutmegFR
 orange blossomFR
 pennyroyalFL/FR
 pineFR
 rosemaryFR
 sageFR
 sassafrasFR
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 anise seed oil
Search Trop  Picture
 apple custard apple plant
Search Trop  Picture
 basil leaf oil
Search Trop  Picture
 basil oil
Search Trop  Picture
 basil plant
Search Trop  Picture
 basil shoot oil
Search Trop  Picture
 bay laurel leaf oil
Search Trop  Picture
 bay laurel plant
Search Trop  Picture
 camphor oil
Search Trop  Picture
 cardamom fruit
Search Trop  Picture
 cardamom seed
Search Trop  Picture
 carrot seed
Search Trop  Picture
 cayenne fruit
Search Trop  Picture
 cinnamomum camphora nees.
Search Trop  Picture
 cinnamon ceylon cinnamon bark oil
Search Trop  Picture
 cinnamon ceylon cinnamon leaf
Search Trop  Picture
 cinnamon ceylon cinnamon oil
Search Trop  Picture
 cinnamon ceylon cinnamon plant
Search Trop  Picture
 cinnamon ceylon cinnamon root bark
Search Trop  Picture
 cinnamon ceylon cinnamon stem bark
Search Trop  Picture
 coriander fruit
Search Trop  Picture
 coriander oil
Search Trop  Picture
 coriander seed oil
Search Trop  Picture
 dill root
Search Trop  Picture
 fennel seed
Search Trop  Picture
 ginger rhizome
Search Trop  Picture
 ginger rhizome oil
Search Trop  Picture
 hyssop flower
Search Trop  Picture
 hyssop leaf
Search Trop  Picture
 hyssop leaf oil
Search Trop  Picture
 hyssop oil
Search Trop  Picture
 lavandula spica
Search Trop  Picture
 lovage root
Search Trop  Picture
 mugwort plant
Search Trop  Picture
 nutmeg seed
Search Trop  Picture
 nutmeg seed oil
Search Trop  Picture
 oregano plant
Search Trop  Picture
 oregano shoot
Search Trop  Picture
 pepper black pepper fruit
Search Trop  Picture
 pepper black pepper seed
Search Trop  Picture
 rosemary
Search Trop  Picture
 rosemary leaf
Search Trop  Picture
 rosemary leaf oil
Search Trop  Picture
 rosemary oil
Search Trop  Picture
 rosemary plant
Search Trop  Picture
 rosemary sap
Search Trop  Picture
 rosemary shoot
Search Trop  Picture
 rosemary shoot oil
Search Trop  Picture
 saffron stigma
Search Trop  Picture
 saffron stigma
Search Trop  Picture
 sage
Search Trop  Picture
 sage leaf
Search Trop  Picture
 sage leaf oil
Search Trop  Picture
 sage oil
Search Trop  Picture
 sage oil dalmatian @ 9.60%
Data  GC  Search Trop  Picture
 sage pericarp oil
Search Trop  Picture
 sassafras officinale
Search Trop  Picture
 savory summer savory plant
Search Trop  Picture
 savory winter savory plant
Search Trop  Picture
 sunflower flower
Search Trop  Picture
 tarragon leaf oil
Search Trop  Picture
 tarragon oil
Search Trop  Picture
 tarragon shoot
Search Trop  Picture
 thyme plant
Search Trop  Picture
 turmeric rhizome
Search Trop  Picture
 turmeric rhizome oil
Search Trop  Picture
 turmeric tuber
Search Trop  Picture
 wormwood wild wormwood plant
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R,4R)-
 bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R,4R)-
(+)-bornan-2-one
(+)-2-bornanone
(1R)- * (+)-2-bornanone
D-2-bornanone
dextro-2-bornanone
D-2-camphanone
dextro-2-camphanone
(+)-camphor
(1R,4R)-(+)-camphor
(1R)-camphor
(1R)- * (+)-camphor
(1R)-(+)-camphor
(R)-camphor
(R)-(+)-camphor
D-camphor
D-(+)-camphor
D-formosa camphor
D-laurel camphor
dextro-(+)-camphor
dextro-formosa camphor
dextro-laurel camphor
japanese camphor
 camphor (gum) powder USP
 camphor (gum) powder, technical
 camphor flake USP24
 camphor gum
 camphor gum natural
 camphor gum synthetic
 camphor powder
 camphor powder natural
 camphor powder natural USP/FCC
 camphor powder synthetic
 camphor-D natural
 camphor, (1R,4R)-(+)-
D-gum camphor
dextro-gum camphor
(R)-1,7,7-trimethyl bicyclo(2.2.1)-2-heptanone
(1R)-1,7,7-trimethyl bicyclo(2.2.1)heptan-2-one
2-keto-1,7,7-trimethyl norcamphane
(R)-1,7,7-trimethylbicyclo(2.2.1)-2-heptanone
(1R,4R)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-one
(1R)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-one
(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
(1R,4R)-1,7,7-trimethylnorbornan-2-one
2-keto-1,7,7-trimethylnorcamphane
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Total synthesis of chiriquitoxin, an analogue of tetrodotoxin isolated from the skin of a dart frog.
PubMed: Hot-spot residues in the cytochrome P450cam-putidaredoxin binding interface.
PubMed: Optically pure, monodisperse cis-oligodiacetylenes: aggregation- induced chirality enhancement.
PubMed: [About flavouring substances and flavouring preparations regulation in the field of manufacturing of flavourings and foodstuffs].
PubMed: Reaction of an "invisible" frustrated N/B Lewis pair with dihydrogen.
PubMed: Nona-coordinated chiral Eu(III) complexes with stereoselective ligand-ligand noncovalent interactions for enhanced circularly polarized luminescence.
PubMed: Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction.
PubMed: In vivo antioxidant activities of essential oils and their constituents from leaves of the Taiwanese Cinnamomum osmophloeum.
PubMed: Spectroscopic evidence for the unusual stereochemical configuration of an endosome-specific lipid.
PubMed: Analysis of volatile compositions of Magnolia biondii pamp by steam distillation and headspace solid phase micro-extraction.
PubMed: Formation of repressor-inducer-operator ternary complex: negative cooperativity of d-camphor binding to CamR.
PubMed: Topological and experimental approach to the pressure-temperature-composition phase diagram of the binary enantiomer system d- and l-camphor.
PubMed: Changing the substrate specificity of P450cam towards diphenylmethane by semi-rational enzyme engineering.
PubMed: Breeding and identification of novel koji molds with high activity of acid protease by genome recombination between Aspergillus oryzae and Aspergillus niger.
PubMed: Improvement of the embryonic stem cell test endpoint analysis by use of field potential detection.
PubMed: Preparation of functionalized cyclic enol phosphates by halogen-magnesium exchange and directed deprotonation reactions.
PubMed: Circularly polarized luminescence of Eu(III) complexes with point- and axis-chiral ligands dependent on coordination structures.
PubMed: Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts.
PubMed: Resolution of planar chiral cationic (eta6-arene)tricarbonylmanganese complexes.
PubMed: Biotransformations of (+/-)-geosmin by terpene-degrading bacteria.
PubMed: D-camphor-crataegus berry extract combination increases blood pressure and cognitive functioning in the elderly - a randomized, placebo controlled double blind study.
PubMed: Skin disposition of d-camphor and l-menthol alone and together.
PubMed: Tetraaquabis(D-camphor-10-sulfonato)calcium(II).
PubMed: A role of the heme-7-propionate side chain in cytochrome P450cam as a gate for regulating the access of water molecules to the substrate-binding site.
PubMed: Diamagnetic lanthanide tris beta-diketonates as organic-soluble chiral NMR shift reagents.
PubMed: D-Camphor-derived triazolium salts for catalytic intramolecular crossed aldehyde-ketone benzoin reactions.
PubMed: Hexaaqua-magnesium(II) bis-(d-camphor-10-sulfonate).
PubMed: Polyploid formation between Aspergillus niger and Trichoderma viride for enhanced citric acid production from cellulose.
PubMed: Preparation of highly conductive, self-assembled gold/polyaniline nanocables and polyaniline nanotubes.
PubMed: Expression, crystallization and preliminary diffraction studies of the Pseudomonas putida cytochrome P450cam operon repressor CamR.
PubMed: [Efficacy and safety of a herbal drug containing hawthorn berries and D-camphor in hypotension and orthostatic circulatory disorders/results of a retrospective epidemiologic cohort study].
PubMed: A randomized trial of Korodin Herz-Kreislauf-Tropfen as add-on treatment in older patients with orthostatic hypotension.
PubMed: Detection of a high-barrier conformational change in the active site of cytochrome P450cam upon binding of putidaredoxin.
PubMed: L358P mutation on cytochrome P450cam simulates structural changes upon putidaredoxin binding: the structural changes trigger electron transfer to oxy-P450cam from electron donors.
PubMed: Crystal structure of P450cin in a complex with its substrate, 1,8-cineole, a close structural homologue to D-camphor, the substrate for P450cam.
PubMed: Discriminative power of an assay for automated in vitro screening of teratogens.
PubMed: NMR study on the structural changes of cytochrome P450cam upon the complex formation with putidaredoxin. Functional significance of the putidaredoxin-induced structural changes.
PubMed: Dose-response related efficacy in orthostatic hypotension of a fixed combination of D-camphor and an extract from fresh crataegus berries and the contribution of the single components.
PubMed: A delicate balance of energetics. Subtleties associated with alpha-ketol-based bridge migration to afford 9-keto-10beta-p-methoxybenzyloxytaxanes.
PubMed: Optical cell with a temperature-control unit for a vacuum-ultraviolet circular dichroism spectrophotometer.
PubMed: Camphor-Crataegus berry extract combination dose-dependently reduces tilt induced fall in blood pressure in orthostatic hypotension.
PubMed: Selection of test chemicals for the ECVAM international validation study on in vitro embryotoxicity tests. European Centre for the Validation of Alternative Methods.
PubMed: Energetic stabilization of d-camphor via weak neutral currents.
PubMed: Adrenodoxin-cytochrome P450scc interaction as revealed by EPR spectroscopy: comparison with the putidaredoxin-cytochrome P450cam system.
PubMed: Putidaredoxin-cytochrome P450cam interaction.
PubMed: X-ray crystal structure and catalytic properties of Thr252Ile mutant of cytochrome P450cam: roles of Thr252 and water in the active center.
PubMed: Roles of the axial push effect in cytochrome P450cam studied with the site-directed mutagenesis at the heme proximal site.
PubMed: In vitro transcriptional analysis of the cytochrome P-450cam hydroxylase operon.
PubMed: Construction and application of MCBL plate for facilitation of chromosome recombination in fungi.
PubMed: Putidaredoxin-cytochrome p450cam interaction. Spin state of the heme iron modulates putidaredoxin structure.
PubMed: Reproductive toxicity studies of D-camphor in rats and rabbits.
PubMed: Preparation of Enantiomerically Enriched (2R,3R)- or (2S,3S)-trans-2,3-Diaryloxiranes via Camphor-Derived Sulfonium Ylides.
PubMed: NMR studies of recombinant cytochrome P450cam mutants.
PubMed: Purification and characterization of a cam repressor (CamR) for the cytochrome P-450cam hydroxylase operon on the Pseudomonas putida CAM plasmid.
PubMed: Substrate interactions in cytochrome P-450: correlation between carbon-13 nuclear magnetic resonance chemical shifts and C-O vibrational frequencies.
PubMed: Thermodynamic aspects of the CO-binding reaction to cytochrome P-450cam. Relevance with their biological significance and structure.
PubMed: Heterologous expression of the cytochrome P450cam hydroxylase operon and the repressor gene of Pseudomonas putida in Escherichia coli.
PubMed: High-pressure flash photolysis study of hemoprotein: effects of substrate analogues on the recombination of carbon monoxide to cytochrome P450CAM.
PubMed: Significant contribution of arginine-112 and its positive charge of Pseudomonas putida cytochrome P-450cam in the electron transport from putidaredoxin.
PubMed: Spectral intermediate in the reaction of ferrous cytochrome P450cam with superoxide anion.
PubMed: Putative functions of phenylalanine-350 of Pseudomonas putida cytochrome P-450cam.
PubMed: Transcription of the cam operon and camR genes in Pseudomonas putida PpG1.
PubMed: Development of bacterial cytochrome P-450(cam) (cytochrome m) production.
PubMed: [d-Camphor reference standard (Control 911) and dl-Camphor Reference Standard (Control 911) of the National Institute of Hygienic Sciences].
PubMed: Observation of the O-O stretching Raman band for cytochrome P-450cam under catalytic conditions.
PubMed: Dopaminergic unique affinity of tetrahydroberberine and l-tetrahydroberberine-d-camphor sulfonate.
PubMed: [d-Camphor Reference Standard (Control 901) and dl-Camphor Reference Standard (Control 901) of National Institute of Hygienic Sciences].
PubMed: Cloning and nucleotide sequences of NADH-putidaredoxin reductase gene (camA) and putidaredoxin gene (camB) involved in cytochrome P-450cam hydroxylase of Pseudomonas putida.
PubMed: Uncoupling of the cytochrome P-450cam monooxygenase reaction by a single mutation, threonine-252 to alanine or valine: possible role of the hydroxy amino acid in oxygen activation.
PubMed: Theoretical study of the product specificity in the hydroxylation of camphor, norcamphor, 5,5-difluorocamphor, and pericyclocamphanone by cytochrome P-450cam.
PubMed: Oxime-metabolizing activity of liver aldehyde oxidase.
PubMed: [D-camphor-beta-sulfonic acid as an ion-pair reagent for the determination of biogenic amines and their metabolites in the rat brain by reverse phase high performance liquid chromatography].
PubMed: Anticonvulsant properties of spirohydantoins derived from optical isomers of camphor.
PubMed: [Central depressant effect of l-tetrahydroberberine-d-camphor sulfonate (THB-CS). Electroencephalographic study].
PubMed: High-pressure investigations of cytochrome P-450 spin and substrate binding equilibria.
PubMed: Novel reactivity of cytochrome P-450-CAM. Methyl hydroxylation of 5,5-difluorocamphor.
PubMed: Regioselectivity in the cytochromes P-450: control by protein constraints and by chemical reactivities.
PubMed: Proton coupling in the ligand-binding reaction of ferric cytochrome P-450 from Pseudomonas putida.
PubMed: Sequential cold-sensitive mutations in Aspergillus fumigatus. II. Analysis by the parasexual cycle.
PubMed: Cytochrome P-450cam and putidaredoxin interaction during electron transfer.
PubMed: Magnetic circular dichroism of Pseudomonas putida cytochrome P-450 in near infrared region.
PubMed: Growth inhibition of Vibrio cholerae by d-camphor.
PubMed: Inhibition of oxidative metabolism in Escherichia coli by d-camphor and restoration of oxidase activity by quinones.
PubMed: Growth inhibition of Escherichia coli strain 82-r by d-camphor.
PubMed: Proton magnetic resonance reveals high-spin iron (II) in ferrous cytochrome P450 cam from Pseudomonas putida.
PubMed: Induction specificity and catabolite repression of the early enzymes in camphor degradation by Pseudomonas putida.
PubMed: Approximation of rotational strengths from molar rotation data and generation of rotatory dispersion curves for d-camphor-10-sulfonate.
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy