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Merck

I3631

Sigma-Aldrich

亚硝酸异戊酯

别名:

亚硝戊酯

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About This Item

线性分子式:
(CH3)2CHCH2CH2ONO
CAS号:
分子量:
117.15
Beilstein:
969510
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:

折射率

n20/D 1.386 (lit.)

沸点

99 °C (lit.)

密度

0.872 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

CC(C)CCON=O

InChI

1S/C5H11NO2/c1-5(2)3-4-8-6-7/h5H,3-4H2,1-2H3

InChI key

OWFXIOWLTKNBAP-UHFFFAOYSA-N

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其他说明

This product has been replaced by 150495-Sigma-Aldrich | Isopentyl nitrite 96%

替代产品

产品编号
说明
价格

警示用语:

Danger

危险分类

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

-4.0 °F - closed cup

闪点(°C)

-20 °C - closed cup

个人防护装备

Eyeshields, Faceshields, 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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Rao M Uppu
Analytical biochemistry, 354(2), 165-168 (2006-06-06)
A method for the synthesis of peroxynitrite is described. It involves nitrosation of H2O2 at pH> or = 12.5 by isoamyl or butyl nitrite in mixed solvents of isopropyl alcohol (IPA) and water at 25+/-1 degrees C. Maximum yields of
Hossein Mehrabi
Ultrasonics sonochemistry, 15(4), 279-282 (2007-10-26)
The reaction of 6-acylmethylphenanthridines with isoamyl nitrite results alpha-oximino-6-acylmethylphenanthridines in 73-95% yields in DMF under ultrasound irradiation. Compared with conventional methods, the main advantages of the present procedure are milder conditions, shorter reaction time and higher yields.
Analysis of alkyl nitrites by capillary gas chromatography-mass spectrometry.
T S Bal et al.
Journal - Forensic Science Society, 28(3), 185-190 (1988-05-01)
R M Uppu et al.
Analytical biochemistry, 236(2), 242-249 (1996-05-01)
A new method for the preparation of high concentrations of peroxynitrite (up to 1 M) is described. The synthesis uses a two-phase system and involves a displacement reaction by the hydroperoxide anion (in the aqueous phase) on isoamyl nitrite (in
E Noack et al.
Basic research in cardiology, 86 Suppl 2, 37-50 (1991-01-01)
All nitrovasodilators act intracellularly by a common molecular mechanism. This is characterized by the release of nitric oxide (NO). They are, thus, prodrugs or carriers of the active principle NO, responsible for endothelial controlled vasodilation. The rate of NO-formation strongly

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