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芳樟醇

analytical standard

同義詞:

(±)-3,7-二甲基-3-羟基-1,6-辛二烯, (±)-二甲基-1,6-辛二烯-3-醇

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About This Item

線性公式:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS號碼:
分子量::
154.25
Beilstein:
1721488
EC號碼:
MDL號碼:
分類程式碼代碼:
85151701
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

蒸汽壓力

0.17 mmHg ( 25 °C)

化驗

≥99.0% (GC)

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.462 (lit.)

bp

194-197 °C/720 mmHg (lit.)

密度

0.87 g/mL at 25 °C (lit.)

應用

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

格式

neat

儲存溫度

2-8°C

SMILES 字串

C\C(C)=C\CCC(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

InChI 密鑰

CDOSHBSSFJOMGT-UHFFFAOYSA-N

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一般說明

Certan Vial
芳樟醇是一种主要的单萜组分,存在于许多芳香族精油中,具有抗炎性质,因此可用于治疗各种急性和慢性疾病。

應用

有关合适仪器技术的更多信息,请参考产品′分析证书。如需进一步支持,请联系技术服务。

其他說明

This compound is commonly found in plants of the genus: cinnamomum salvia thymus

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

171.0 °F - Pensky-Martens closed cup

閃點(°C)

77.2 °C - Pensky-Martens closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

Linalool modifies the nicotinic receptor-ion channel kinetics at the mouse neuromuscular junction
Re.L, et al.
Pharmacological Research, 42(2), 177-181 (2000)
Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils
Peana.T.A, et al.
Phytomedicine, 9(8), 721-726 (2002)
L Re et al.
Pharmacological research, 42(2), 177-182 (2000-07-11)
Linalool is a monoterpene compound reported to be a major component of essential oils in various aromatic species. Several linalool-producing species are used in traditional medical systems. Among these is Aeolanthus suaveolens G. Dom (Labiatae) which is used as an
Ali M Al Hazmi et al.
Organic letters, 16(19), 5104-5107 (2014-09-17)
The permanganate-mediated oxidative cyclization of a series of 2-methylenehept-5-eneoates bearing different chiral auxiliaries was investigated, leading to the discovery of trans-2-tritylcyclohexanol (TTC) as a highly effective chiral controller for the formation of the 2,5-substituted THF diol product with high diastereoselectivity
Michiko Miyashita et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 53, 174-179 (2012-12-12)
As malignant neoplasm is a major public health problem, there is a need for the development of a novel modulator that enhances antitumor activity and reduces adverse reactions to antitumor agents. In this study, the effects of some volatile oil

文章

-Cymene; Linalool; Menthol; α-Terpineol; Menthyl acetate

條款

-(+)-Limonene, purum, ≥98.0% (sum of enantiomers, GC); Geranyl tiglate; α-Terpineol, natural, ≥96%, FCC, FG; Geranyl formate; α-Pinene

-Pinocarveol; Menthol; (+)-Terpinen-4-ol; α-Terpineol; (±)-α-Terpinyl acetate, predominantly α-isomer; Germacrene D

-Cymene; (−)-Menthone; α-Terpineol, natural, ≥96%, FCC, FG; Terpinolene; β-Bourbonene; 1-Octen-3-ol; β-Caryophyllene; Linalool; α-Terpinene; (−)-Menthol

Cymene; 4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran; Linalool; Menthol; Menthone; Menthyl acetate; Germacrene D; Bicyclogermacrene; Thymol

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