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W224707

Sigma-Aldrich

L-Carveol, mixture of cis and trans

≥95%, FG

Synonym(s):

(−)-Carveol, mixture of isomers, p-Mentha-6,8-dien-2-ol

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
99-48-9
Molecular Weight:
152.23
FEMA Number:
2247
EC Number:
202-757-4
Council of Europe no.:
2027
MDL number:
MFCD00869995
UNSPSC Code:
12164502
PubChem Substance ID:
24900945
Flavis number:
2.062
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

Assay

≥95%

optical activity

[α]22/D −115°, c = 1 in chloroform

composition

contains IFRA restricted Carvone

refractive index

n20/D 1.496 (lit.)

bp

226-227 °C/751 mmHg (lit.)

density

0.958 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

carvone

Organoleptic

minty; herbaceous

SMILES string

CC(=C)[C@@H]1CC=C(C)C(O)C1

InChI

1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10?/m1/s1

InChI key

BAVONGHXFVOKBV-YHMJZVADSA-N

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General description

L-Carveol, mixture of cis and trans is a cyclic terpene alcohol that can be used as a flavoring agent and fragrance ingredient.{80

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

208.4 °F - closed cup

Flash Point(C)

98 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN7741
SHBN7743
SHBM8346
SHBM8345
MKCH2169

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Burdock GA
Encyclopedia of Food and Color Additives, 1, 520-521 (1997)
Moshe Parnas et al.
Cell calcium, 45(3), 300-309 (2009-01-13)
Transient receptor potential (TRP) channels are essential components of biological sensors that detect changes in the environment in response to a myriad of stimuli. A major difficulty in the study of TRP channels is the lack of pharmacological agents that
Jenna L E Morrish et al.
Biotechnology and bioengineering, 101(5), 946-956 (2008-06-12)
In an effort to improve reactor performance and process operability, the microbial biotransformation of (-)-trans-carveol to (R)-(-)-carvone by hydrophobic Rhodococcus erythropolis DCL14 was carried out in a two phase partitioning bioreactor (TPPB) with solid polymer beads acting as the partitioning
Tomoko Iizuka et al.
Drugs in R&D, 11(2), 191-205 (2011-06-18)
In Japan, when pharmaceutical companies launch a new drug, they are obligated to conduct a post-marketing survey to evaluate the safety and efficacy of the drug in accordance with Good Post-Marketing Surveillance Practice under Article 14-4 (re-examination) of the Pharmaceutical
Jenna L E Morrish et al.
Biotechnology and bioengineering, 101(4), 768-775 (2008-05-15)
The microbial biotransformation of (-)-trans-carveol to the flavor and fragrance compound (R)-(-)-carvone by Rhodococcus erythropolis DCL14 was carried out in a 3 L two phase partitioning bioreactor with an immiscible liquid second phase in an effort to improve upon the
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