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)
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。
signalword
Warning
hcodes
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
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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