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Merck

W263516

Sigma-Aldrich

L-芳樟醇

greener alternative

natural, ≥95%, FG

别名:

(-)-芳樟醇, (R)-(-)-3,7-二甲基-1,6-辛二烯-3-醇

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About This Item

线性分子式:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS号:
分子量:
154.25
FEMA號碼:
2635
Beilstein:
1721487
EC號碼:
歐洲委員會號碼:
61
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
2.013
NACRES:
NA.21

等級

FG
Fragrance grade
Halal
Kosher
natural

品質等級

agency

follows IFRA guidelines

法律遵循

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

化驗

≥95%

光學活性

[α]20/D −19.8°, neat

環保替代產品特色

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

折射率

n20/D 1.4615 (lit.)

bp

198 °C (lit.)

密度

0.862 g/mL at 20 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

linalool

環保替代類別

感官的

woody; floral

SMILES 字串

C\C(C)=C\CC[C@@](C)(O)C=C

InChI

1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3/t10-/m0/s1

InChI 密鑰

CDOSHBSSFJOMGT-JTQLQIEISA-N

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一般說明

L-芳樟醇是茉莉花茶、云杉精油荔枝嫩叶的主要挥发性化合物。
我们竭诚为您带来满足绿色替代产品四大类别要求的替代产品。本品为生物基产品,在“危险性较小的化学合成”和“使用可再生原料”绿色化学原则方面取得了重大进步。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

166.3 °F - closed cup

閃點(°C)

74.6 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Volatile components of Litchi chinensis Sonn. leaf oil extracts obtained by simultaneous distillation extraction.
Wang YJ, et al.
Journal of Essential Oil-Bearing Plants, 16(2), 161-165 (2013)
Maged E Mohamed et al.
Biomolecules, 10(11) (2020-11-01)
The monoterpene linalool is a well-known essential oil component produced by several aromatic plants. Cisplatin is a widely used anticancer drug that produces many side effects, particularly nephrotoxicity. Here, we aimed to inspect linalool's protective activity against cisplatin-induced nephrotoxicity and
Sedative effects of the jasmine tea odor and (R)-(?)-linalool, one of its major odor components, on autonomic nerve activity and mood states
Kuroda K, et al.
European Journal of Applied Physiology, 95(2-3), 107-114 (2005)
Behavioral and electrophysiological responses of Tetropium fuscum (Coleoptera: Cerambycidae) to pheromone and spruce volatiles.
Silk PJ, et al.
Environmental Entomology, 39(6), 1997-2005 (2010)
Nobuhisa Nitta et al.
Microbial cell factories, 20(1), 54-54 (2021-03-04)
Linalool, an acyclic monoterpene alcohol, is extensively used in the flavor and fragrance industries and exists as two enantiomers, (S)- and (R)-linalool, which have different odors and biological properties. Linalool extraction from natural plant tissues suffers from low product yield.

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