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Merck

400890

Sigma-Aldrich

顺式-2-丁烯

≥99%

别名:

(2Z)-2-Butene, (Z)-2-Butene, Z-Butene, cis-1,2-Dimethylethylene, cis-2-Butylene

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About This Item

线性分子式:
CH3CH=CHCH3
CAS号:
分子量:
56.11
Beilstein:
1361341
EC號碼:
MDL號碼:
分類程式碼代碼:
12142100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

2 (vs air)

蒸汽壓力

1414 mmHg ( 21 °C)

化驗

≥99%

形狀

gas

自燃溫度

615 °F

expl. lim.

9.7 %

bp

3.7 °C (lit.)

mp

−139 °C (lit.)

SMILES 字串

[H]\C(C)=C(/[H])C

InChI

1S/C4H8/c1-3-4-2/h3-4H,1-2H3/b4-3-

InChI 密鑰

IAQRGUVFOMOMEM-ARJAWSKDSA-N

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應用

cis-2-Butene is an unsaturated olefinic hydrocarbon used as a precursor in the polymerization of gasoline. It is also used to synthesize butadiene and other aliphatic C4/C5 organic molecules. It is also employed as a cross-linking agent.

包裝

Supplied in a Sure/Pac cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

法律資訊

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

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说明
价格

校準器

产品编号
说明
价格

軟管倒鉤

产品编号
说明
价格

象形圖

FlameGas cylinder

訊號詞

Danger

危險聲明

防範說明

危險分類

Flam. Gas 1 - Press. Gas Liquefied gas

儲存類別代碼

2A - Gases

水污染物質分類(WGK)

WGK 3

閃點(°F)

10.4 °F - closed cup

閃點(°C)

-12 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)


分析证书(COA)

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在文件库中查找您最近购买产品的文档。

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Basic organic chemicals
Polymer, 117-141 (2002)
Competition and miscibility of isodimorphism and their effects on band spherulites and mechanical properties of poly (butylene succinate-co-cis-butene succinate) unsaturated aliphatic copolyesters
Yu Y, et al.
Polymer, 150, 52-63 (2018)
Franz Worek et al.
Archives of toxicology, 86(9), 1379-1386 (2012-03-23)
The reactivation of organophosphorus compound (OP)-inhibited acetylcholinesterase (AChE) by oximes is inadequate in case of different OP nerve agents. This fact led to the synthesis of numerous novel oximes by different research groups in order to identify more effective reactivators.
Nadiya Bakhiya et al.
Archives of toxicology, 84(7), 563-578 (2010-03-20)
Furan is formed during commercial or domestic thermal treatment of food. The initial surveys of furan concentrations in heat-treated foods, published by European and US authorities, revealed the presence of relatively high furan levels in coffee, sauces, and soups. Importantly
J T Groves et al.
Progress in clinical and biological research, 274, 509-524 (1988-01-01)
A cytochrome P-450 LM2 reconstituted system mediated expoxidations of small terminal alkenes to the corresponding alkyloxiranes. This oxidation was accompanied by a stereoselective proton exchange of the E proton. Propene was oxidized in D2O to trans-3-deuterio-2-methyloxirane, and E-1-deuteriopropene was epoxidized

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