Merck
CN

388246

Sigma-Aldrich

二甲胺 溶液

2.0 M in methanol

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别名:
N,N-Dimethylamine
线性分子式:
(CH3)2NH
CAS号:
分子量:
45.08
Beilstein:
605257
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

形式

liquid

质量水平

浓度

1.90 -2.20 M (NaOH, titration)
2.0 M in methanol

密度

0.775 g/mL at 25 °C

SMILES字符串

CNC

InChI

1S/C2H7N/c1-3-2/h3H,1-2H3

InChI key

ROSDSFDQCJNGOL-UHFFFAOYSA-N

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一般描述

Dimethylamine, a secondary amine, is used as a raw material for the production of many agrichemicals and pharmaceuticals. The solvents dimethylformamide (DMF) and dimethylacetamide (DMA) are derived from dimethylamine. It is also used as a precursor for the preparation of amido derivatives.

应用

Dimethylamine can be used as a precursor for the preparation of a number of chemical building blocks such as dimethyl(3-chloropropyl)amine , 2-chloro-N,N-dimethylethanimidamide , and 4, 6-dichloro-2-(dimethylamino)-1,3,5-triazine .

包装

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

法律信息

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

相关产品

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 1 - STOT SE 3

靶器官

Eyes, Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

41.0 °F - closed cup

闪点(°C)

5 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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Methylamines
van Gysel A B and Musin W
Ullmann's Encyclopedia of Industrial Chemistry (1997)
4-Dimethylaminobutyraldehyde diethyl acetal
FENG R-l, et al.
JOURNAL-SHANDONG UNIVERSITY OF SCIENCE AND TECHNOLOGY NATURAL SCIENCE, 5 (2011)
Synthesis of 3-{4-[4-dimethylamino-6-(4-methyl-2-oxo-2H-chromen-7-yloxy)-[1, 3, 5] triazin-2-ylamino]-phenyl}-2-phenyl-5-(4-pyridin-2-yl-piperazin-1-ylmethyl)-thiazolidin-4-one and their biological evaluation
Patel D, et al.
Medicinal Chemistry Research, 21(10), 2926-2944 (2012)
Synthesis of 2-amino-4-imino-4, 5-dihydrothiazoles from N-sulfonyl-α -chloroamidines and thiourea
Abdelaal SM and Bauer L
Journal of Heterocyclic Chemistry, 25(6), 1849-1856 (1988)
Gerhild Zauner et al.
Biochimica et biophysica acta, 1820(9), 1420-1428 (2011-08-02)
Analysis of protein glycosylation is an important first step towards establishing the functions of glycans in health and disease. In contrast to N-glycans which are generally enzymatically released for analysis, there is no corresponding enzyme for O-glycan liberation. Therefore, O-glycans

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