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Merck
CN
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安全信息

270032

Sigma-Aldrich

N,N′-二甲基乙二胺

85%

别名:

1,2-双(甲氨基)乙烷

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About This Item

线性分子式:
CH3NHCH2CH2NHCH3
CAS号:
110-70-3
分子量:
88.15
Beilstein:
878142
EC 号:
203-793-3
MDL编号:
MFCD00008290
UNSPSC代码:
12352100
PubChem化学物质编号:
24856188
NACRES:
NA.22

质量水平

100

方案

85%

表单

liquid

折射率

n20/D 1.431 (lit.)

沸点

119 °C (lit.)

密度

0.819 g/mL at 20 °C (lit.)

官能团

amine

SMILES字符串

CNCCNC

InChI

1S/C4H12N2/c1-5-3-4-6-2/h5-6H,3-4H2,1-2H3

InChI key

KVKFRMCSXWQSNT-UHFFFAOYSA-N

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应用

N,N′-Dimethylethylenediamine was used to enhance CO2 adsorption. It was incorporated into H3[(Cu4Cl)3(BTTri)8 (CuBTTri; H3BTTri = 1,3,5-tri(1H-1,2,3-triazol-4-yl)benzene), a water-stable, triazolate-bridged framework, to form a metal–organic framework for CO2 separation.

其他说明

残留物为 N-甲基乙二胺

象形图

FlameCorrosion
GHS02,GHS05

警示用语：

Danger

危险声明

H226,H314

危险分类

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

78.8 °F - closed cup

闪点(°C)

26 °C - closed cup

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCC0805
MKBZ2469V
MKBW9237V
MKBQ7303V
MKBJ8791V

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Enhanced carbon dioxide capture upon incorporation of N, N?-dimethylethylenediamine in the metal?organic framework CuBTTri.
McDonald TM, et al.
Chemical Science, 2(10), 2022-2028 (2011)
Deprotection of N(in)-formyl group on tryptophan by application of new reagent, 1,2-dimethylethylendiamine in aqueous solution.
Takenao Odagami et al.
Advances in experimental medicine and biology, 611, 159-160 (2009-04-30)
J T Hwang et al.
Nucleic acids research, 27(19), 3805-3810 (1999-09-11)
The formal C1'-oxidation product, 2-deoxyribonolactone, is formed as a result of DNA damage induced via a variety of agents, including gamma-radiolysis and the enediyne antitumor antibiotics. This alkaline labile lesion may also be an intermediate during DNA damage induced by
Kim A Lennox et al.
Oligonucleotides, 16(1), 26-42 (2006-04-06)
A wide variety of modified oligonucleotides have been tested as antisense agents. Each chemical modification produces a distinct profile of potency, toxicity, and specificity. Novel cationic phosphoramidate-modified antisense oligonucleotides have been developed recently that have unique and interesting properties. We
Ghotas Evindar et al.
The Journal of organic chemistry, 71(5), 1802-1808 (2006-02-25)
A general method for the formation of benzoxazoles via a copper-catalyzed cyclization of ortho-haloanilides is reported. This approach complements the more commonly used strategies for benzoxazole formation which require 2-aminophenols as substrates. The reaction involves an intramolecular C-O cross-coupling of
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