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Merck
CN

471208

乙胺 溶液

66.0-72.0% in H2O

别名:

一乙胺, 氨基乙烷

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关于此项目

线性分子式:
C2H5NH2
化学文摘社编号:
分子量:
45.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
505933
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产品名称

乙胺 溶液, 66.0-72.0% in H2O

InChI

1S/C2H7N/c1-2-3/h2-3H2,1H3

SMILES string

CCN

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

concentration

66.0-72.0% in H2O

density

0.81 g/mL at 20 °C

functional group

amine

Quality Level

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Application

乙胺溶液用于制备 N-乙基三嗪哌嗪共聚物 (ETPC),作为疏水阻燃材料。它也用于聚四甲基氧化物/二氧化硅杂化复合材料的改性。

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 1

flash_point_f

71.6 °F

flash_point_c

22 °C

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:

分析证书(COA)

Lot/Batch Number

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Modification of an inorganic-organic hybrid composite: effect of ethylamine.
Brennan, Anthony B and Miller, Thomas M
Chemistry of Materials, 6(3), 262-267 (1994)
Synthesis of N-ethyl triazine-piperazine copolymer and flame retardancy and water resistance of intumescent flame retardant polypropylene.
Yang, Kun et al.
Polymer Degradation and Stability, 98(7), 1397-1406 (2013)
Stacey F Bent et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(3), 956-960 (2010-11-12)
Surface functionalization of semiconductors has been the backbone of the newest developments in microelectronics, energy conversion, sensing device design, and many other fields of science and technology. Over a decade ago, the notion of viewing the surface itself as a
Paige E Mahaney et al.
Journal of medicinal chemistry, 51(13), 4038-4049 (2008-06-19)
Further exploration of the cycloalkanol ethylamine scaffold, of which venlafaxine ( 1) is a member, was undertaken to develop novel and selective norepinephrine reuptake inhibitors (NRIs) for evaluation in a variety of predictive animal models. These efforts led to the
Riccardo Di Corato et al.
ACS nano, 5(2), 1109-1121 (2011-01-12)
Trifunctional polymer nanobeads are prepared by destabilization of a mixture of magnetic nanoparticles, quantum dots, and an amphiphilic polymer, followed by functionalization of the bead surface with folic acid molecules. The distribution of the nanoparticles within the nanobeads can be

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