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270032

N,N′-二甲基乙二胺

Name: <I>N</I>,<I>N</I>′-二甲基乙二胺
Brand: ALDRICH

85%

别名:

1,2-双(甲氨基)乙烷

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关于此项目

线性分子式:

CH₃NHCH₂CH₂NHCH₃

化学文摘社编号:

110-70-3

分子量:

88.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24856188

EC Number:

203-793-3

Beilstein/REAXYS Number:

878142

MDL number:

MFCD00008290

Assay:

85%

Form:

liquid

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属性

Quality Level

100

assay

85%

form

liquid

refractive index

n20/D 1.431 (lit.)

bp

119 °C (lit.)

density

0.819 g/mL at 20 °C (lit.)

functional group

amine

SMILES string

CNCCNC

InChI

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

InChI key

KVKFRMCSXWQSNT-UHFFFAOYSA-N

说明

Application

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.

Other Notes

残留物为 N-甲基乙二胺

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pictograms

GHS02,GHS05

signalword

Danger

hcodes

H226,H314

pcodes

P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

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

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

78.8 °F - closed cup

flash_point_c

26 °C - closed cup

ppe

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

法规信息

危险化学品

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历史批次信息供参考:

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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)

Characterization of modified antisense oligonucleotides in Xenopus laevis embryos.

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

Parallel synthesis of a library of benzoxazoles and benzothiazoles using ligand-accelerated copper-catalyzed cyclizations of ortho-halobenzanilides.

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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全球贸易项目编号

货号	GTIN
270032-25G	04061826141762
270032-100G	04061826141755