(4R,6R)-carveol

(4R,6R)-p-mentha-1,8-dien-6-ol

CAS: 2102-59-2 C10 H16 O MW: 152.23672000 minty

Identification

Name(4R,6R)-carveol
IUPAC(1R,5R)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol
CAS Number2102-59-2
EINECS218-270-5
FDA UNIIOOZ105PLI9
Molecular FormulaC10 H16 O
Molecular Weight152.23672000
Nikkaji NumberJ9.138C
Beilstein2042973
CoE Number2027

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.95210 @ 25.00 °C.
Refractive Index 1.49720 @ 20.00 °C.
Boiling Point 101.00 °C. @ 10.00 mm Hg, 108.00 °C. @ 16.00 mm Hg
Vapor Pressure 0.012000 mmHg @ 25.00 °C. (est)
Flash Point 196.00 °F. TCC ( 91.20 °C. ) (est)
logP (o/w) 2.819 (est)
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesperfuming agents

Organoleptic Properties

Odor Description at 100.00 %.

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryflavor and fragrance agents
RIFM Fragrance Material Safety AssessmentSearch
maximum skin levels for fine fragrances0.0200 % and are based on the assumption that the fragrance mixture is used at 20% in a consumer product (IFRA Use Level Survey).
use level in formulae for use in cosmetics0.0200 %
Dermal Systemic Exposure in Cosmetic Products0.0005 mg/kg/day

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Potential Uses

None Found

Natural Occurrence

orange fruit spearmint

Synonyms

(-)-(4R,6R)-cis- carveol (-)-cis- carveol (1R,5R)-(-)-cis- carveol (1R)-cis- carveol (4R,6R)-cis- carveol cis-(-)- carveol L-cis- carveol laevo-cis- carveol 2- cyclohexen-1-ol, 2-methyl-5- (1-methylethenyl)-, cis- 2- cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, (1R,5R)- 2- cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, cis- (4R,6R)-p- mentha-1,8-dien-6-ol (2R,4R)-(-)-p- mentha-6,8-dien-2-ol (2R,4R)-(-)-para- mentha-6,8-dien-2-ol (1R-cis)-2- methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol (1R,5R)-2- methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol (1R-cis)-2- methyl-5-isopropenyl-2-cyclohexen-1-ol (1R,5R)-2- methyl-5-prop-1-en-2-ylcyclohex-2-en-1-ol PubMed: GC-MS characterisation and antibacterial activity evaluation of Nigella sativa oil against diverse strains of Salmonella. PubMed: Chemical composition, cytotoxicity and in vitro antitrypanosomal and antiplasmodial activity of the essential oils of four Cymbopogon species from Benin. PubMed: Chemical composition and insecticidal activity of the essential oil of Illicium pachyphyllum fruits against two grain storage insects. PubMed: Chemical composition and larvicidal activity of essential oil from Mentha spicata (Linn.) against three mosquito species. PubMed: Insecticidal activity of essential oil of Carum Carvi fruits from China and its main components against two grain storage insects. PubMed: Enhanced bioproduction of carvone in a two-liquid-phase partitioning bioreactor with a highly hydrophobic biocatalyst. PubMed: Regio- and stereoselective fungal oxyfunctionalisation of limonenes. PubMed: Analysis of volatile components from Ziziphora taurica subsp. taurica by steam distillation, superheated-water extraction, and direct thermal desorption with GCxGC-TOFMS. PubMed: Repellency of essential oils of some Kenyan plants against Anopheles gambiae. PubMed: Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage. PubMed: Sensitive biomonitoring of monoterpene exposure by gas chromatographic-mass spectrometric measurement of hydroxy terpenes in urine. PubMed: Hydroxylation of specifically deuterated limonene enantiomers by cytochrome p450 limonene-6-hydroxylase reveals the mechanism of multiple product formation. PubMed: Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from mint (Mentha) species: evidence for catalysis within sterically constrained active sites. PubMed: Effects of R-(+)-limonene on submerged cultures of the terpene transforming basidiomycete Pleurotus sapidus.