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Merck
CN

53675

α-蛇麻烯

≥96.0% (GC)

别名:

α-丁子香烯, 反,反,反-2,6,6,9-四甲基-1,4,8-环十一烷三烯

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关于此项目

经验公式(希尔记法):
C15H24
化学文摘社编号:
分子量:
204.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
229-816-7
Beilstein/REAXYS Number:
3240075
MDL number:
Assay:
≥96.0% (GC)
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InChI key

FAMPSKZZVDUYOS-HRGUGZIWSA-N

InChI

1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3/b11-6+,13-7+,14-10+

SMILES string

C\C1=C/CC(C)(C)\C=C\C\C(C)=C\CC1

assay

≥96.0% (GC)

refractive index

n20/D 1.503 (lit.)

bp

166-168 °C (lit.)

density

0.889 g/mL at 20 °C (lit.)

storage temp.

2-8°C

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General description

αα-蛇麻烯是在Cordia verbenacea精油中存在的倍半萜。

Application

αα-蛇麻烯还可用于通过氧化法形成二次有机气溶胶。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Rafael C Dutra et al.
The Journal of pharmacy and pharmacology, 61(2), 243-250 (2009-01-31)
The objective of this work was to investigate the antiulcerogenic and anti-inflammatory activities of the essential oil from Pterodon emarginatus seeds. The following tests were used: ulcers induced by ethanol, indometacin and HCl/ethanol, and pleurisy induced by carrageenan in Swiss
Fengnian Yu et al.
Planta, 227(6), 1291-1299 (2008-02-15)
Shampoo ginger (Zingiber zerumbet Smith) has a high content and large variety of terpenoids in the essential oil of its rhizome. Here, we report on the isolation of a cDNA clone (ZSS1) encoding alpha-humulene synthase, a possible key enzyme of
Ping-Chuan Jiang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 32(8), 1224-1227 (2009-12-08)
To study the volatile oil of Murraya exotica. The volatile oil of Murraya exotica was extracted by steam-stilling and was identified by GC-MS-DS. More than 90 compounds were separated, and 59 compounds were identified, accounting for 93.9% of the total
Shin-Pin Chen et al.
Chemical & pharmaceutical bulletin, 57(2), 162-166 (2009-02-03)
A novel skeletal norhumulene (1) and six xeniaphyllane-derived compounds, including norditerpenoids (2, 3) and diterpenoids (4-7), were isolated from the EtOAc extract of the Formosan soft coral Sinularia gibberosa. Their structures were elucidated by spectroscopic analysis. In vitro cytotoxic evaluation
Secondary organic aerosol formation from the oxidation of a series of sesquiterpenes: α-cedrene, β-caryophyllene, α-humulene and α-farnesene with O3, OH and NO3 radicals
Jaoui M, et al.
Environmental Chemistry, 10(3), 178-193 (2013)

实验方案

-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

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