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Key Documents

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W224707

Sigma-Aldrich

L-Carveol, mixture of cis and trans

≥95%, FG

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C10H16O
Número de CAS:
99-48-9
Peso molecular:
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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

208.4 °F - closed cup

flash_point_c

98 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Burdock GA
Encyclopedia of Food and Color Additives, 1, 520-521 (1997)
Staffan Johansson et al.
Chemical research in toxicology, 22(11), 1774-1781 (2009-09-04)
The widespread use of scented products causes an increase of allergic contact dermatitis to fragrance compounds in Western countries today. Many fragrance compounds are prone to autoxidation, forming hydroperoxides as their primary oxidation products. Hydroperoxides are known to be strong
Juan Carlos R Gonçalves et al.
European journal of pharmacology, 645(1-3), 108-112 (2010-07-31)
Carvone (p-mentha-6,8-dien-2-one) is a monoterpene ketone found as the main active component of various essential oils. It is obtained by distillation and occurs naturally as the enantiomers (+)- and (-)-carvone. Our group have shown that the in vivo antinociceptive activity
Devin R Polichuk et al.
Phytochemistry, 71(11-12), 1264-1269 (2010-07-14)
The major components of the isoprenoid-rich essential oil of Artemisia annua L. accumulate in the subcuticular sac of glandular secretory trichomes. As part of an effort to understand isoprenoid biosynthesis in A. annua, an expressed sequence tag (EST) collection was
S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S88-S90 (2008-07-22)
A toxicologic and dermatologic review of laevo-carveol when used as a fragrance ingredient is presented.
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