EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

dextro-camphor
D-camphor

Supplier Sponsors

Fragrance Demo Formulas
Name:(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
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.
 
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
 
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)
Odor sample from: Berje Inc.
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).
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
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
 
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
 
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: --
 
Safety References:
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
 
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
 
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
 
Potential Blenders and core components note
For Odor
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 extract
FL/FR
cistus ladaniferus resinoid
FL/FR
animal
1-oxa
spiro-4,7-dodecane
FR
anise
anise seed oil
FL/FR
star
anise seed oil china
FL/FR
anise seed oil colombia
FL/FR
star
anise seed oil spain
FL/FR
balsamic
iso
amyl benzoate
FL/FR
amyris wood oil
FL/FR
benzoin
FL/FR
siam
benzoin resinoid
FL/FR
benzyl benzoate
FL/FR
benzyl salicylate
FL/FR
dextro,laevo-iso
borneol
FL/FR
iso
bornyl acetate
FL/FR
bornyl acetate
FL/FR
iso
bornyl formate
FL/FR
iso
bornyl propionate
FL/FR
cedar forest fragrance
FR
conifer acetate
FR
fir balsam absolute
FR
frankincense absolute
FL/FR
3-
phenyl propyl alcohol
FL/FR
camphoreous
cyclohexanol
FL/FR
melaleuca viridiflora leaf oil
FR
citrus
methyl heptenone
FL/FR
neroli ketone
FR
creamy
veratraldehyde
FL/FR
earthy
2-
octanone
FL/FR
fatty
decanol
FL/FR
floral
aglaia odorata absolute
FR
alpha-
amyl cinnamaldehyde
FL/FR
iso
amyl salicylate
FL/FR
bigarade oxide
FR
iso
butyl salicylate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
ho leaf oil
FR
karo karounde absolute
FR
karo karounde absolute replacer
FR
lavender oil
FL/FR
nonanol
FL/FR
petitgrain bigarade oil
FL/FR
phenethyl alcohol
FL/FR
sambucus nigra flower oil CO2 extract
FR
5-
tricyclodecenyl acetate
FR
fruity
allyl cyclohexyl propionate
FL/FR
3-
benzyl-4-heptanone
FL/FR
green
iso
cyclocitral (IFF)
FL/FR
dicyclopentadiene propionate
FR
alpha-
hexyl cinnamaldehyde dimethyl acetal
FR
para-
methyl hydratropaldehyde
FL/FR
seaweed absolute (fucus vesiculosus et serratus)
FL/FR
hay
tobacco leaf absolute
FL/FR
herbal
ajowan seed oil
FL/FR
1-
allyl-2,2,7,7-tetramethyl cycloheptanol
FR
angelica archangelica seed extract
FL/FR
anthemis nobilis flower oil roman
FL/FR
artemisia vestita wall. leaf oil
FR
bornyl 2-methyl butyrate
FL/FR
bornyl butyrate
FL/FR
beta-
bourbonene
FL/FR
3-
butyl phthalide
FL/FR
calamintha clinopodium oil
FR
cardamom liquid resin
FR
carum carvi fruit oil
FL/FR
1,8-
cineole
FL/FR
dill seed oil
FL/FR
dill seed oil CO2 extract
FL/FR
eucalyptus globulus oil
FL/FR
eucalyptus oil replacer
FR
herbal undecanone
FR
immortelle flower oil
FL/FR
abrialis
lavandin oil
FL/FR
lavandin water absolute
FL/FR
spike
lavender oil
FL/FR
2-
methyl butyl salicylate
FL/FR
origanum oil greece
FL/FR
alpha-
pinene
FL/FR
pinocarveol
FL/FR
piperitone
FL/FR
rosemary oil spain
FL/FR
rosemary oleoresin
FL/FR
safranal
FL/FR
white
thyme oil
FL/FR
thyme oil (thymus zygis gracillis) spain
FL/FR
red
thyme oil india
FL/FR
red
thyme oil spain
FL/FR
thyme oil wild or creeping
FL/FR
thymol
FL/FR
mentholic
peppermint cyclohexanone
FL/FR
minty
mint fragrance
FR
mint specialty
FR
pennyroyal oil
FL/FR
mossy
veramoss (IFF)
FR
musk
angelica root absolute
FL/FR
naphthyl
1-
methyl naphthalene
FL/FR
nutty
pentanoic acid, 3-methyl-2-oxo-, ethyl ester
FL/FR
orris
para-iso
propyl acetophenone
FL/FR
powdery
para-
anisyl alcohol
FL/FR
spicy
bayberry fragrance
FR
cardamom oil replacer
FR
cassia bark oil china
FL/FR
cinnamon acrolein
FL/FR
clove bud oil
FL/FR
clove leaf oil
FL/FR
elettaria cardamomum seed oil
FL/FR
elettaria cardamomum seed oil guatemala
FL/FR
ginger oleoresin africa
FL/FR
ginger root absolute
FL/FR
ginger root oil cochin
FL/FR
maja fragrance
FR
myrcene
FR
2-
octanol
FL/FR
black
pepper absolute
FL/FR
white
pepper oil
FL/FR
black
pepper oil
FL/FR
black
pepper oleoresin
FL/FR
4-iso
propyl-2-cyclohexenone
FL/FR
terpenic
cypress leaf oil
FR
frankincense oil
FL/FR
juniperus communis fruit oil
FL/FR
thujonic
cedarleaf oil western red
FR
sage oil dalmatian
FL/FR
common
tansy flower oil argentina
FL/FR
common
tansy leaf oil dutch
FR
woody ketone
FL/FR
tonka
tonka bean absolute
FR
waxy
ethyl laurate
FL/FR
woody
angelica archangelica root extract
FL/FR
angelica archangelica root tincture
FL/FR
angelica archangelica root water
FL/FR
cadinene
FL/FR
camphene
FL/FR
(+)-
camphene
FL/FR
cypress essence
FR
dalbergia sissoo leaf oil
FR
dihydro-alpha-terpinyl acetate
FR
fougere woody fragrance
FR
laitone
FR
manevoro oil
FR
marine formate
FR
melaleuca bracteata leaf oil
FR
methyl cedryl ketone
FL/FR
patchouli ethanone
FR
patchouli oil
FL/FR
polylimonene
FL/FR
santol pentenol
FR
spruce needle oil canada
FL/FR
tetrahydromugol
FR
thuja occidentalis leaf oil
FL/FR
vetiver oil haiti
FL/FR
woody acetate
FR
For Flavor
No flavor group found for these
angelica archangelica root extract
FL/FR
angelica archangelica root oil CO2 extract
FL/FR
angelica archangelica root tincture
FL/FR
angelica archangelica root water
FL/FR
benzoin
FL/FR
bornyl 2-methyl butyrate
FL/FR
bornyl butyrate
FL/FR
beta-
bourbonene
FL/FR
3-
butyl phthalide
FL/FR
delta-
cadinene
FL
(+)-
camphene
FL/FR
cistus ladaniferus resinoid
FL/FR
cyclohexanol
FL/FR
2-
methyl butyl salicylate
FL/FR
3-
methyl cyclohexanone
FL
1-
methyl pyrrole
FL
polylimonene
FL/FR
4-iso
propyl-2-cyclohexenone
FL/FR
seaweed absolute (fucus vesiculosus et serratus)
FL/FR
woody ketone
FL/FR
aldehydic
aldehydic
nonanal (aldehyde C-9)
FL/FR
anise
anise seed oil
FL/FR
star
anise seed oil china
FL/FR
anise seed oil colombia
FL/FR
star
anise seed oil spain
FL/FR
balsamic
siam
benzoin resinoid
FL/FR
benzyl benzoate
FL/FR
benzyl salicylate
FL/FR
iso
bornyl propionate
FL/FR
camphoreous
dextro,laevo-iso
borneol
FL/FR
bornyl acetate
FL/FR
camphene
FL/FR
pinocarveol
FL/FR
citrus
petitgrain bigarade oil
FL/FR
cooling
iso
butyl salicylate
FL/FR
spike
lavender oil
FL/FR
creamy
veratraldehyde
FL/FR
dairy
2-
octanone
FL/FR
fatty
10-
undecenal (aldehyde C-11 undecylenic)
FL/FR
floral
phenethyl alcohol
FL/FR
fruity
allyl cyclohexyl propionate
FL/FR
iso
amyl benzoate
FL/FR
para-
anisyl alcohol
FL/FR
3-
benzyl-4-heptanone
FL/FR
grassy
tobacco leaf absolute
FL/FR
green
iso
amyl salicylate
FL/FR
iso
cyclocitral (IFF)
FL/FR
methyl heptenone
FL/FR
para-
methyl hydratropaldehyde
FL/FR
herbal
ajowan seed oil
FL/FR
angelica archangelica seed extract
FL/FR
anthemis nobilis flower oil roman
FL/FR
cardamom distillates
FL
cardamom flavor
FL
carum carvi fruit oil
FL/FR
celery seed oleoresin
FL
dill seed oil
FL/FR
dill seed oil CO2 extract
FL/FR
eucalyptus flavor
FL
eucalyptus globulus oil
FL/FR
immortelle flower oil
FL/FR
abrialis
lavandin oil
FL/FR
lavandin water absolute
FL/FR
lavender oil
FL/FR
origanum oil greece
FL/FR
rosemary oil spain
FL/FR
rosemary oleoresin
FL/FR
white
thyme oil
FL/FR
thyme oil (thymus zygis gracillis) spain
FL/FR
red
thyme oil india
FL/FR
red
thyme oil spain
FL/FR
thyme oil wild or creeping
FL/FR
medicinal
frankincense absolute
FL/FR
mentholic
peppermint cyclohexanone
FL/FR
minty
1,8-
cineole
FL/FR
pennyroyal oil
FL/FR
piperitone
FL/FR
musk
angelica root absolute
FL/FR
naphthyl
1-
methyl naphthalene
FL/FR
nutty
pentanoic acid, 3-methyl-2-oxo-, ethyl ester
FL/FR
phenolic
thymol
FL/FR
pine
spruce beer flavor
FL
soapy
dodecanal (aldehyde C-12 lauric)
FL/FR
spicy
cassia bark oil china
FL/FR
cinnamon acrolein
FL/FR
clove bud oil
FL/FR
clove leaf oil
FL/FR
elettaria cardamomum seed oil
FL/FR
elettaria cardamomum seed oil guatemala
FL/FR
ginger oleoresin africa
FL/FR
ginger root absolute
FL/FR
ginger root oil cochin
FL/FR
2-
octanol
FL/FR
black
pepper absolute
FL/FR
black
pepper oil
FL/FR
white
pepper oil
FL/FR
black
pepper oleoresin
FL/FR
3-
phenyl propyl alcohol
FL/FR
para-iso
propyl acetophenone
FL/FR
terpenic
juniperus communis fruit oil
FL/FR
thujonic
sage oil dalmatian
FL/FR
common
tansy flower oil argentina
FL/FR
tropical
alpha-
amyl cinnamaldehyde
FL/FR
waxy
decanal (aldehyde C-10)
FL/FR
decanol
FL/FR
ethyl laurate
FL/FR
alpha-
hexyl cinnamaldehyde
FL/FR
nonanol
FL/FR
woody
amyris wood oil
FL/FR
iso
bornyl acetate
FL/FR
iso
bornyl formate
FL/FR
cadinene
FL/FR
frankincense oil
FL/FR
methyl cedryl ketone
FL/FR
patchouli oil
FL/FR
alpha-
pinene
FL/FR
safranal
FL/FR
spruce needle oil canada
FL/FR
thuja occidentalis leaf oil
FL/FR
vetiver oil haiti
FL/FR
 
Potential Uses:
FRbasil oil replacer
FL/FRcamphor tree bark
FRcologne
 disinfectants
FRfloral
FRlavandin
FRlavender
FL/FRlavender spike lavender
FRnutmeg
FRorange blossom
FL/FRpennyroyal
FRpine
FRrosemary
FRsage
FRsassafras
FRwoody
 
Occurrence (nature, food, other):note
 anise seed oil
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 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
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 rosemary shoot oil
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 saffron stigma
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 saffron stigma
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 sage
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 sage leaf
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 sage leaf oil
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 sage oil
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 sage oil dalmatian @ 9.60%
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 sage pericarp oil
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 sassafras officinale
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 savory summer savory plant
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 savory winter savory plant
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 sunflower flower
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 tarragon leaf oil
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 tarragon oil
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 tarragon shoot
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 thyme plant
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 turmeric rhizome
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 turmeric rhizome oil
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 turmeric tuber
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 wormwood wild wormwood plant
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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
 

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.
 
Notes:
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