跳转至内容
Merck
CN

360554

Sigma-Aldrich

硝基甲烷

ACS reagent, ≥95%

登录查看公司和协议定价

关于此项目

经验公式(希尔记法):
CH3NO2
CAS Number:
分子量:
61.04
Beilstein:
1698205
EC 号:
MDL编号:
UNSPSC代码:
12352102
PubChem化学物质编号:
NACRES:
NA.21
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

等级

ACS reagent

质量水平

蒸汽密度

2.1 (vs air)

蒸汽压

2.7 mmHg ( 20 °C)

方案

≥95%

表单

liquid

自燃温度

784 °F

expl. lim.

7.3 %, 33 °F

dilution

(for analytical testing)

杂质

≤0.05% water

颜色

APHA: ≤10

折射率

n20/D 1.382 (lit.)

pH值(酸碱度)

6.4 (20 °C, 0.01 g/L)

沸点

101.2 °C (lit.)

mp

−29 °C (lit.)

密度

1.127 g/mL at 25 °C (lit.)

适用性

clear for appearance

SMILES字符串

C[N+]([O-])=O

InChI

1S/CH3NO2/c1-2(3)4/h1H3

InChI key

LYGJENNIWJXYER-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

硝基甲烷是一种脂肪族硝基化合物,通常用作化学加工和分析的溶剂。
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

应用

硝基甲烷可作为溶剂用于:
  • FeCl3-催化的吲哚与醇傅-克烷基化反应。
  • 钴催化的醛肟脱水生成腈反应。
  • 醇生成羰基化合物的化学选择性氧化反应。
  • 金催化的芳基取代炔烃的氢芳基化反应。

警示用语:

Warning

危险分类

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 3 - Repr. 2

储存分类代码

4.1A - Other explosive hazardous materials

WGK

WGK 2

闪点(°F)

95.0 °F - closed cup

闪点(°C)

35 °C - closed cup

法规信息

危险化学品
易制爆化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

The catalytic chemistry of nitromethane over Co-ZSM5 and other catalysts in connection with the methane-NOxSCR reaction.
Cowan AD, et al.
J. Catal., 176(2), 329-343 (1998)
Metal ion encapsulation: cobalt cages derived from polyamines, formaldehyde, and nitromethane.
Geue RJ, et al.
Journal of the American Chemical Society, 106(19), 5478-5488 (1984)
Benedek Vakulya et al.
Organic letters, 7(10), 1967-1969 (2005-05-07)
Cinchona alkaloid-derived chiral bifunctional thiourea organocatalysts were synthesized and applied in the Michael addition between nitromethane and chalcones with high ee and chemical yields.
Atanu Bhattacharya et al.
The Journal of chemical physics, 136(2), 024321-024321 (2012-01-21)
Decomposition of electronically excited nitro-containing molecules with different X-NO(2) (X = C, N, O) moieties has been intensively investigated over the past decades; however, their decomposition behavior has not previously been compared and contrasted. Comparison of their unimolecular decomposition behavior
Wenguo Yang et al.
Chemistry, an Asian journal, 7(4), 771-777 (2012-02-10)
Through the cleavage of the C-C bond, the first catalytic tandem conjugate addition-elimination reaction of Morita-Baylis-Hillman C adducts has been presented. Various S(N)2'-like C-, S-, and P-allylic compounds could be obtained with exclusive E configuration in good to excellent yields.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持