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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编号:
2247
EC 号:
202-757-4
欧洲委员会编号:
2027
MDL编号:
MFCD00869995
UNSPSC代码:
12164502
PubChem化学物质编号:
24900945
Flavis编号:
2.062
NACRES:
NA.21
Agency:
follows IFRA guidelines

主要文件

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生物来源

synthetic

质量水平

300
400

等级

FG
Fragrance grade
Halal
Kosher

Agency

follows IFRA guidelines

管理合规性

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

方案

≥95%

旋光性

[α]22/D −115°, c = 1 in chloroform

组成

contains IFRA restricted Carvone

折射率

n20/D 1.496 (lit.)

沸点

226-227 °C/751 mmHg (lit.)

密度

0.958 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

carvone

性状检查

minty; herbaceous

SMILES字符串

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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相关类别

一般描述

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

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

208.4 °F - closed cup

闪点(°C)

98 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SHBR9060
SHBR8439
SHBP9154
SHBP9150
SHBP9159

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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
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
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