葑醇

更新时间：2025-08-25 19:02:50

葑醇结构式	常用名	葑醇	英文名	Fenchol
	CAS号	1632-73-1	分子量	154.249
	密度	1.0±0.1 g/cm3	沸点	202.9±8.0 °C at 760 mmHg
	分子式	C₁₀H₁₈O	熔点	35-40ºC
	MSDS	中文版美版	闪点	73.9±0.0 °C
	符号	GHS07	信号词	Warning

葑醇用途

Fenchyl alcohol 是从道格拉斯松叶精油中的一种单萜醇,能作为香精。Fenchyl alcohol 对绵羊和鹿瘤胃微生物活性具很强的抑制作用。

中文名	葑醇
英文名	(-)-endo-fenchol
中文别名	1,3,3-三甲基双环[2,2,1]庚-2-醇 \| 小茴香醇 \| 1,3,3-三甲基-2-降冰片
英文别名	更多

描述	Fenchyl alcohol 是从道格拉斯松叶精油中的一种单萜醇,能作为香精。Fenchyl alcohol 对绵羊和鹿瘤胃微生物活性具很强的抑制作用。
相关类别	研究领域 >> 感染信号通路 >> 其他 >> 其他
参考文献	[1]. Api AM, et al. RIFM fragrance ingredient safety assessment, Fenchyl alcohol, CAS registry number 1632-73-1. Food Chem Toxicol. 2015 Oct;84 Suppl:S25-32. [2]. Oh HK, et al. Effect of Various Essential Oils Isolated from Douglas Fir Needles upon Sheep and Deer Rumen Microbial Activity. Appl Microbiol. 1967 Jul;15(4):777-84.

描述

Fenchyl alcohol 是从道格拉斯松叶精油中的一种单萜醇,能作为香精。Fenchyl alcohol 对绵羊和鹿瘤胃微生物活性具很强的抑制作用。

相关类别

研究领域 >> 感染

信号通路 >> 其他 >> 其他

参考文献

[1]. Api AM, et al. RIFM fragrance ingredient safety assessment, Fenchyl alcohol, CAS registry number 1632-73-1. Food Chem Toxicol. 2015 Oct;84 Suppl:S25-32.

[2]. Oh HK, et al. Effect of Various Essential Oils Isolated from Douglas Fir Needles upon Sheep and Deer Rumen Microbial Activity. Appl Microbiol. 1967 Jul;15(4):777-84.

密度	1.0±0.1 g/cm3
沸点	202.9±8.0 °C at 760 mmHg
熔点	35-40ºC
分子式	C₁₀H₁₈O
分子量	154.249
闪点	73.9±0.0 °C
精确质量	154.135757
PSA	20.23000
LogP	2.71
InChIKey	IAIHUHQCLTYTSF-UHFFFAOYSA-N
SMILES	CC12CCC(C1)C(C)(C)C2O
外观性状	无色至淡黄色固体或液体
蒸汽压	0.1±0.9 mmHg at 25°C
折射率	1.502
储存条件	2-8°C

符号	GHS07
信号词	Warning
危害声明	H315-H319-H335
警示性声明	P261-P305 + P351 + P338
危害码 (欧洲)	Xi
风险声明 (欧洲)	36/37/38
安全声明 (欧洲)	22-24/25-26
危险品运输编码	UN 1325 4.1/PG 2
WGK德国	3
RTECS号	DT5080000

Chocolate smells pink and stripy: Exploring olfactory-visual synesthesia.

Cogn Neurosci 6 , 77-88, (2015)

Odors are often difficult to identify, and can be perceived either via the nose or mouth ("flavor"; not usually perceived as a "smell"). These features provide a unique opportunity to contrast concept...

[GC-MS analysis and inhibitory activity of the essential oil extracted from the leaves of Lindera communis].

Zhong Yao Cai 22(3) , 128-31, (1999)

The essential oil isolated from the dried leaves of Lindera communis was analyzed by means of gas chromatography-mass(GC-MS) technique, the structures of 23 chemical components were identified from it...

Biosynthesis of monoterpenes. Enantioselectivity in the enzymatic cyclization of linalyl pyrophosphate to (-)-endo-fenchol.

J. Biol. Chem. 260(26) , 13901-8, (1985)

The conversion of geranyl pyrophosphate to (-)-endo-fenchol is considered to proceed by the initial isomerization of the substrate to (-)-(3R)-linalyl pyrophosphate and the subsequent cyclization of t...

2-Fenchanol

1,3,3-trimethyl-2-norbornanol

1-Hydroxyfenchane

D-Fenchyl alcohol

fenchyl alcohol

FEMA 2480

FENCHOL

1,3,3-Trimethylbicyclo[2.2.1]heptan-2-ol