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Merck
CN

W224707

L-香芹醇，顺式和反式混合物

≥95%, FG

别名:

(-)-香芹醇，异构体混合物, 葛缕醇

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关于此项目

经验公式（希尔记法）:
C10H16O
化学文摘社编号:
99-48-9
分子量:
152.23
FEMA Number:
2247
Council of Europe no.:
2027
UNSPSC Code:
12164502
PubChem Substance ID:
24900945
Flavis number:
2.062
EC Number:
202-757-4
NACRES:
NA.21
MDL number:
MFCD00869995
Organoleptic:
minty; herbaceous
Grade:
FG, Fragrance grade, Halal, Kosher
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens

主要文件

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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

biological source

synthetic

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

Quality Level

300, 400

相关类别

General description

L -香芹酚，顺和反式的混合物，是一种环萜烯醇，可用作调味剂和香料成分。{80

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBT4550
SHBR9060
SHBR8439
SHBP9154
SHBP9150

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Burdock GA
Encyclopedia of Food and Color Additives, 1, 520-521 (1997)
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
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.
M J van der Werf et al.
Microbiology (Reading, England), 146 ( Pt 5), 1129-1141 (2000-06-01)
Rhodococcus erythropolis DCL14 assimilates all stereoisomers of carveol and dihydrocarveol as sole source of carbon and energy. Induction experiments with carveol- or dihydrocarveol-grown cells showed high oxygen consumption rates with these two compounds and with carvone and dihydrocarvone. (Dihydro)carveol-grown cells
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
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