Merck
CN
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文件

安全信息

W285609

Sigma-Aldrich

α-水芹烯

≥75%, stabilized

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别名:
2-甲基-5-（1-甲基乙基）-1，3-环己二烯
经验公式（希尔记法）:
C10H16
CAS号:
99-83-2
分子量:
136.23
FEMA编号:
2856
EC 号:
202-792-5
欧洲委员会编号:
2117
MDL编号:
MFCD00040419
PubChem化学物质编号:
24901345
Flavis编号:
1.006

生物来源

synthetic

质量水平

400

等级

Halal
Kosher

reg. compliance

FDA 21 CFR 172.515

检测方案

≥75%

旋光性

[α]20/D −139 to −110°, neat

包含

alpha-tocopherol as additive

折射率

n20/D 1.474 (lit.)

密度

0.85 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

性状检查

spicy; woody

SMILES string

CC(C)C1CC=C(C)C=C1

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4-6,8,10H,7H2,1-3H3

InChI key

OGLDWXZKYODSOB-UHFFFAOYSA-N

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相关类别

免责声明

For R&D or non-EU Food use. Not for retail sale.

象形图

FlameHealth hazard
GHS02,GHS08

警示用语：

Danger

危险声明

H226 - H304

危险分类

Asp. Tox. 1 - Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

116.6 °F - closed cup

闪点(°C)

47 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

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Kazuhiro Okamoto et al.
Organic letters, 10(19), 4387-4389 (2008-09-06)
Chiral dienes possessing the bicyclo[2.2.2]octadiene framework were prepared readily through the [4 + 2] cycloaddition of ( R)-alpha-phellandrene with methyl propiolate as the key step. Diene 9, substituted with a tertiary alcohol on one of the two double bonds, is
S Foss et al.
Systematic and applied microbiology, 21(2), 237-244 (1998-08-15)
Four pseudomonad strains 51Men, 54Pin, 62Car and 65Phen were recently isolated on the monoterpenes (+)-menthene, alpha-pinene, 2-carene and alpha-phellandrene as sole carbon source and nitrate as electron acceptor. These bacteria were characterised. The motile, mesophilic, Gram-negative rods had a strictly
Gökalp İşcan et al.
Chemistry & biodiversity, 9(8), 1525-1532 (2012-08-18)
Terpene derivatives converted by microbial biotransformation constitute an important resource for natural pharmaceutical, fragrance, and aroma substances. In the present study, the monoterpene α-phellandrene was biotransformed by 16 different strains of microorganisms (bacteria, fungi, and yeasts). The transformation metabolites were
David F Lima et al.
The Journal of pharmacy and pharmacology, 64(2), 283-292 (2012-01-10)
The aim of this work was to investigate the antinociceptive property of α-phellandrene (α-PHE) in experimental nociception models and possible mechanisms involved. Mass spectrometry was used to evaluate the purity and molecular mass of α-PHE. Macrophages from mice peritoneal cavity
M Miyazawa et al.
Journal of agricultural and food chemistry, 48(7), 2893-2895 (2000-07-18)
gamma-Terpinene was mixed in artificial diet at a concentration of 1 mg/g of diet, and the diet was fed to the last instar larvae of common cutworm (Spodoptera litura). Metabolites were recovered from frass and analyzed spectroscopically. gamma-Terpinene was transformed
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