dextro-dihydrocarvone
carvone, dihydro-
 
Notes:
Flavouring agent with spearmint-like flavour
  • BOC Sciences
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      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.
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      Product(s):
      7764-50-3 Cyclohexanone,2-methyl-5-(1-methylethenyl)-
       
  • 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.
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      DIHYDROCARVONE
      DIHYDROCARVONE NATURAL
       
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    • 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.
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      Product(s):
      04-18500 DIHYDROCARVONE
      04-18520 DIHYDROCARVONE NATURAL NEAT
       
  • Sigma-Aldrich
  • Synerzine
    • Synerzine, Inc.
      Innovation. Customization. Aroma Ingredients.
      Synerzine is a leading supplier of flavor and fragrance ingredients.
      Synerzine expresses what we have grown to embody as an organization - the synergy and connection between raw ingredients, science, technology, and the final product. Our experienced team is passionate about bringing our customers high-quality innovative ingredients that they can trust.
      Building upon our 44 year history, the Synerzine team provides customers around the globe with convenient access to over 1200 high-quality aroma ingredients. We actively engage with customers to add a wide array of new products and services on a regular basis. Our aim is to delight every customer with our exceptional services, large product selection, customization and the highest quality and safety standards. We provide our customers with true value designed to help them bring their products to market faster.
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      Product(s):
      W0394 D-Dihydrocarvone (mixed isomers)
       
Synonyms   Articles   Notes   Search
CAS Number: 7764-50-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 231-857-0
FDA UNII: YQS5CW1O1J
Nikkaji Web: J87.284I
MDL: MFCD00001636
CoE Number: 11703
XlogP3-AA: 2.70 (est)
Molecular Weight: 152.23672000
Formula: C10 H16 O
NMR Predictor: Predict (works with chrome or firefox)
EFSA/JECFA Comments: At least 77%; secondary components 10-15% dihydrocarveol; 5-6% carvone; 2-3% carveol. (JECFA)
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: 377  dihydrocarvone
DG SANTE Food Flavourings: 07.128  dihydrocarvone
FEMA Number: 3565 dihydrocarvone
FDA:No longer provide for the use of these seven synthetic flavoring substances
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 97.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.92300 to 0.92800 @  25.00 °C.
Pounds per Gallon - (est).: 7.680 to  7.722
Refractive Index: 1.46900 to 1.47200 @  20.00 °C.
Optical Rotation: +14 to +18
Boiling Point: 87.00 to  88.00 °C. @ 6.00 mm Hg
Boiling Point: 222.00 to  223.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.107000 mmHg @ 25.00 °C. (est)
Vapor Density: 5.2 ( Air = 1 )
Flash Point: 192.00 °F. TCC ( 88.89 °C. )
logP (o/w): 2.850
Soluble in:
 alcohol
 fixed oils
 water, 1020 mg/L @ 15 °C (exp)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: minty
 
 warm  herbal  spearmint  
Odor Description:
at 100.00 %. 
warm powerful herbal spearmint
 
 cooling  minty  woody  terpenic  herbal  hay  bread rye bread  camphoreous  
Odor Description:
Cooling, minty, woody, terpy, herbal, hay, rye bread and camphoreous
Mosciano, Gerard P&F 23, No. 2, 43, (1998)
 
 
Flavor Type: green
 
 green  spicy  minty  woody  camphoreous  
Taste Description:
at 4.00 ppm.  
Green, spicy, minty and woody with a camphoreous nuance
Mosciano, Gerard P&F 23, No. 2, 43, (1998)
 
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:
BOC Sciences
For experimental / research use only.
Cyclohexanone,2-methyl-5-(1-methylethenyl)-
Indenta Group
Dihydro Carvone
Lluch Essence
DIHYDROCARVONE NATURAL
Lluch Essence
DIHYDROCARVONE
Penta International
DIHYDROCARVONE NATURAL NEAT
Penta International
DIHYDROCARVONE
Reincke & Fichtner
D-Dihydrocarvone (mixture of isomeres)
Santa Cruz Biotechnology
For experimental / research use only.
(+)-Dihydrocarvone, mixture of isomers
Sigma-Aldrich
D-Dihydrocarvone, mixture of isomers, ≥97%, FCC, FG
Odor: herbaceous; minty
Certified Food Grade Products
Sigma-Aldrich
D-Dihydrocarvone, mixture of isomers, natural, 97%, FG
Odor: herbaceous; spearmint
Synerzine
D-Dihydrocarvone (mixed isomers)
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Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 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.
Human Experience:
20 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 18, Pg. 665, 1980.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 18, Pg. 665, 1980.

subcutaneous-mouse LD50 2900 mg/kg
BEHAVIORAL: ANTICONVULSANT BEHAVIORAL: SLEEP
Journal of the American Pharmaceutical Association, Scientific Edition. Vol. 46, Pg. 77, 1957.

Inhalation Toxicity:
Not determined
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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-dihydrocarvone usage levels up to:
  10.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.012 (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: 11
Click here to view publication 11
 average usual ppmaverage maximum ppm
baked goods: -15.70000
beverages(nonalcoholic): -2.70000
beverages(alcoholic): -4.00000
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -7.30000
fruit ices: --
gelatins / puddings: -4.70000
granulated sugar: --
gravies: --
hard candy: --
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: -14.00000
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):
Flavouring Group Evaluation 9, Revision 1: (FGE.09 Rev1)[1] - Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical groups 8 and 30, and an ester of a phenol carboxylic acid from chemical group 25 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 9, Revision 2 (FGE.09Rev2): Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical group 8 and 30, and an ester of a phenol derivative from chemical group 25
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 7764-50-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 24473
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1993
WGK Germany: 2
 2-methyl-5-prop-1-en-2-ylcyclohexan-1-one
Chemidplus: 0007764503
RTECS: OT0305000 for cas# 7764-50-3
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References:
Leffingwell: Chirality or Article
 2-methyl-5-prop-1-en-2-ylcyclohexan-1-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 7764-50-3
Pubchem (cid): 24473
Pubchem (sid): 134990145
Pherobase: View
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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
CHEBI: View
KEGG (GenomeNet): C18018
HMDB (The Human Metabolome Database): HMDB36079
FooDB: FDB014914
Export Tariff Code: 2914.29.5000
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
 wasabi root 
balsamic
isobornyl acetateFL/FR
 bornyl acetateFL/FR
isobornyl propionateFL/FR
 croton glabellus bark extractFL/FR
 frankincense absoluteFL/FR
 juniper berry absoluteFL/FR
camphoreous
 bornyl ethyl ether 
beta-homocyclocitralFL/FR
citrus
 bergamot oil turkeyFL/FR
 trimethyl cyclohexeneFR
 verbena absolute franceFL/FR
coconut
(R)-gamma-hexalactone 
floral
 cilantro herb oil egyptFL/FR
beta-ocimeneFL/FR
fruity
para-anisyl methyl ketoneFL/FR
(E)-beta-damasconeFL/FR
2,2,4-trimethyl-1,3-oxathiane 
hay
 woodruff absoluteFR
herbal
 anethum graveolens herb oilFL/FR
1,4-cineoleFL/FR
 coriander oleoresinFL/FR
 dehydroxylinalool oxideFL/FR
isodihydrolavandulolFR
(Z)-isodihydrolavandulyl acetateFR
 geranic oxideFL/FR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
 lavender concreteFL/FR
spike lavender oilFL/FR
 melaleuca linariifolia oilFR
para-menthane-3,8-diolFL/FR
 origanum oil terpenesFR
curled parsley seed oilFL/FR
 pinocarveolFL/FR
 sabinene hydrateFL/FR
 terpinoleneFL/FR
 thyme oil wild or creepingFL/FR
leathery
black tea leaf absoluteFL/FR
mentholic
 cornmint oilFL/FR
 cornmint oil indiaFL/FR
dextro,laevo-mentholFL/FR
(±)-isomenthoneFL/FR
 menthyl acetate racemicFL/FR
minty
dextro-carvoneFL/FR
homomentholFL/FR
(±)-menthoneFL/FR
homomenthyl acetateFL/FR
laevo-menthyl lactateFL/FR
 pennyroyal oil fractionsFL/FR
 peppermint absoluteFL/FR
 peppermint oil americaFL/FR
 peppermint oil idahoFL/FR
isopropyl tiglateFL/FR
(-)-isopulegolFL/FR
isopulegolFL/FR
naphthyl
ortho-methyl anisoleFL/FR
pine
 dipentene terpene hydrocarbon byproductsFR
spicy
alpha-amyl cinnamyl alcoholFL/FR
 angelica oilFL/FR
isobutyl angelateFL/FR
 carrot weed oilFL/FR
beta-caryophylleneFL/FR
 caryophylleneFL/FR
 croton eluteria bark oilFL/FR
 cuminaldehydeFL/FR
 ginger root oil brazilFL/FR
 ginger root oil chinaFL/FR
 ginger root oil cochinFL/FR
(R)-gamma-heptalactone 
 hollyberry fragranceFR
 myrceneFR
 nutmeg absoluteFL/FR
 origanum majorana oilFL/FR
black pepper oilFL/FR
sulfurous
 mango thiolFL/FR
terpenic
 juniperus communis fruit oilFL/FR
laevo-limoneneFL/FR
alpha-phellandreneFL/FR
gamma-terpineneFL/FR
tonka
 deertongue oleoresinFR
 flouve absoluteFR
woody
isobornyl isovalerateFL/FR
para-tert-butyl cyclohexanoneFR
 campheneFL/FR
(-)-myrtenol 
lariciu pine needle oilFR
 sandalwood oilFL/FR
 sandalwood oil CO2 extractFL/FR
alpha-terpineneFL/FR
 
For Flavor
 
No flavor group found for these
 croton glabellus bark extractFL/FR
(R)-gamma-heptalactone 
(R)-gamma-hexalactone 
para-menthane-3,8-diolFL/FR
 menthyl acetate racemicFL/FR
2,2,4-trimethyl-1,3-oxathiane 
2,4,4-trimethyl-1,3-oxathianeFL
balsamic
isobornyl propionateFL/FR
 juniper berry absoluteFL/FR
camphoreous
 bornyl acetateFL/FR
 bornyl ethyl ether 
 campheneFL/FR
 geranic oxideFL/FR
6-hydroxydihydrotheaspirane (mixture of isomers)FL/FR
ortho-methyl anisoleFL/FR
 pinocarveolFL/FR
citrus
 bergamot oil turkeyFL/FR
 verbena absolute franceFL/FR
cooling
1,4-cineoleFL/FR
beta-homocyclocitralFL/FR
spike lavender oilFL/FR
dextro,laevo-mentholFL/FR
homomenthyl acetateFL/FR
laevo-menthyl lactateFL/FR
 peppermint oil americaFL/FR
 sabinene hydrateFL/FR
fruity
(E)-beta-damasconeFL/FR
green
isobutyl angelateFL/FR
 carrot weed oilFL/FR
beta-ocimeneFL/FR
isophoroneFL
isopropyl tiglateFL/FR
 wasabi root 
herbal
 anethum graveolens herb oilFL/FR
 cilantro herb oil egyptFL/FR
 coriander oleoresinFL/FR
 lavender concreteFL/FR
 origanum majorana oilFL/FR
curled parsley seed oilFL/FR
 thyme oil wild or creepingFL/FR
meaty
2-methyl 3-(methyl thio) furanFL
medicinal
 frankincense absoluteFL/FR
mentholic
 cornmint oilFL/FR
minty
dextro-carvoneFL/FR
 cornmint oil indiaFL/FR
homomentholFL/FR
(±)-menthoneFL/FR
(±)-isomenthoneFL/FR
(-)-myrtenol 
 pennyroyal oil fractionsFL/FR
 peppermint absoluteFL/FR
 peppermint oil idahoFL/FR
(-)-isopulegolFL/FR
isopulegolFL/FR
spicy
alpha-amyl cinnamyl alcoholFL/FR
 angelica oilFL/FR
para-anisyl methyl ketoneFL/FR
 caryophylleneFL/FR
beta-caryophylleneFL/FR
 croton eluteria bark oilFL/FR
 cuminaldehydeFL/FR
 ginger root oil brazilFL/FR
 ginger root oil chinaFL/FR
 ginger root oil cochinFL/FR
 nutmeg absoluteFL/FR
black pepper oilFL/FR
sulfurous
 mango thiolFL/FR
tea
black tea leaf absoluteFL/FR
terpenic
 juniperus communis fruit oilFL/FR
laevo-limoneneFL/FR
para-menthatrieneFL
alpha-phellandreneFL/FR
alpha-terpineneFL/FR
gamma-terpineneFL/FR
woody
isobornyl acetateFL/FR
isobornyl isovalerateFL/FR
 dehydroxylinalool oxideFL/FR
 sandalwood oilFL/FR
 sandalwood oil CO2 extractFL/FR
 terpinoleneFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 angelicaFL/FR
 hay new mown hayFR
 herbalFR
 mintFR
 spiceFR
 woodyFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 amomum testaceum ridl. fruit oil malaysia @ 0.30%
Data  GC  Search Trop  Picture
 caraway oil
Search Trop  Picture
 caraway plant
Search Trop  Picture
 caraway seed
Search Trop  Picture
 caraway seed oil
Search Trop  Picture
 celery seed
Search Trop  Picture
 celery seed oil
Search Trop  Picture
 celery seed oil CO2 extract india @ 0.02%
Data  GC  Search Trop  Picture
 celery seed oil india @ 0.07%
Data  GC  Search Trop  Picture
 dill herb
Search Trop  Picture
 dill leaf
Search Trop  Picture
 dill leaf oil
Search Trop  Picture
 dill oil
Search Trop  Picture
 dill root
Search Trop  Picture
 dill seed oil
Search Trop  Picture
 mikan peel oil @ trace%
Data  GC  Search Trop  Picture
 patchouli oil china @ 0.01%
Data  GC  Search Trop  Picture
 pepper black pepper fruit
Search Trop  Picture
 pepper black pepper seed
Search Trop  Picture
 peppermint leaf
Search Trop  Picture
 spearmint leaf
Search Trop  Picture
 spearmint oil
Search Trop  Picture
 spearmint shoot
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 carvone, dihydro-
 cyclohexanone, 2-methyl-5-(1-methylethenyl)-
 di hydro carvone
 dihydrocarvone
D-dihydrocarvone
D-dihydrocarvone, mixture of isomers
p-menth-8-en-2-one
para-menth-8-en-2-one
p-menth-8(9)-en-2-one
8-p-menthen-2-one
2-methyl-5-(1-methyl vinyl) cyclohexan-1-one
2-methyl-5-(1-methylethenyl)cyclohexanone
2-methyl-5-(1-methylvinyl)cyclohexan-1-one
2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-one
2-methyl-5-(prop-1-en-2-yl)cyclohexanone
2-methyl-5-isopropenylcyclohexanone
2-methyl-5-prop-1-en-2-ylcyclohexan-1-one
5-isopropenyl-2-methylcyclohexanone
3-isopropenyl-6-methyl cyclohexanone
3-isopropenyl-6-methylcyclohexanone
Synonyms   Articles   Notes   Search   Top
Synonyms   Articles   Notes   Search   Top
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