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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


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分析证书(COA)

Lot/Batch Number

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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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