Merck
CN
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文件

221457

Sigma-Aldrich

N,N-二甲基羟胺 盐酸盐

99%

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线性分子式:
(CH3)2NOH · HCl
CAS号:
16645-06-0
分子量:
97.54
Beilstein:
3905683
EC 号:
240-691-8
MDL编号:
MFCD00012600
PubChem化学物质编号:
24853241
NACRES:
NA.22

检测方案

99%

形式

solid

mp

107-109 °C (lit.)

SMILES字符串

Cl[H].CN(C)O

InChI

1S/C2H7NO.ClH/c1-3(2)4;/h4H,1-2H3;1H

InChI key

HWWVAHCWJLGKLW-UHFFFAOYSA-N

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相关类别

应用

N，N-二甲基羟胺盐酸盐用于合成 4，4-二甲基-2，5，5-三苯基-1.3-二氧杂-4-氮杂-2-硼-2-硼酸环戊烷。boratacyclopentane它也被用作聚合物链终止剂。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319

危险分类

Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Structural studies of organoboron compounds. XVI. Preparation and crystal and molecular structures of 4, 4-dimethyl-2, 5, 5-triphenyl-1, 3-dioxa-4-azonia-2-bora-5-boratacyclopentane and 4, 4, 5, 5-tetramethyl-2, 2-diphenyl-1, 3-dioxa-4-azonia-2-boratacyclopentane.
Canadian Journal of Chemistry, 62(5), 838-844 (1984)
A R Tunoori et al.
Organic letters, 2(25), 4091-4093 (2000-12-12)
[structure] The reagent [bis(2-methoxyethyl)amino]sulfur trifluoride (Deoxo-Fluor reagent) converts carboxylic acids to the corresponding acid fluorides, which then react with N,N-dimethylhydroxylamine to give the corresponding Weinreb amides in high yields. The reaction proceeds without racemization when optically active acids are used
Hana Popelkova et al.
Photosynthesis research, 110(2), 111-121 (2011-11-02)
The photosystem II (PSII) manganese-stabilizing protein (PsbO) is known to be the essential PSII extrinsic subunit for stabilization and retention of the Mn and Cl(-) cofactors in the oxygen evolving complex (OEC) of PSII, but its function relative to Ca(2+)
K Stolze et al.
Free radical research communications, 8(2), 123-131 (1990-01-01)
Nitroxide radicals have been detected in the methemoglobin formation reaction between oxyhemoglobin and the substituted hydroxylamine compounds, N-methylhydroxylamine and N,N-dimethylhydroxylamine, by ESR spectroscopy. The stability of these nitroxide radicals was considerably higher than that of the NH2O. radical derived from
A A Spooren et al.
Archives of toxicology, 71(5), 299-305 (1997-01-01)
Hydroxylamine (HYAM, HONH2) and some of its derivatives are known to cause erythrotoxic effects both in vitro and in vivo. Previous studies have shown that the primary in vitro effect of HYAM and O-ethyl hydroxylamine (OEH) is methaemoglobin formation, leading
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