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Merck
CN

110167

Sigma-Aldrich

乙醇胺

≥99%, liquid, ReagentPlus®

别名:

2-氨基乙基醇, 2-氨基乙醇, ETA, MEA, MEA 90, MEA-LCI, 单乙醇胺

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关于此项目

线性分子式:
NH2CH2CH2OH
化学文摘社编号:
分子量:
61.08
Beilstein:
505944
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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产品名称

乙醇胺, ReagentPlus®, ≥99%

蒸汽密度

2.1 (vs air)

蒸汽压

0.2 mmHg ( 20 °C)

产品线

ReagentPlus®

方案

≥99%

表单

liquid

自燃温度

1436 °F

expl. lim.

17 %

折射率

n20/D 1.454 (lit.)

沸点

170 °C (lit.)
69-70 °C/10 mmHg

mp

10-11 °C (lit.)

溶解性

water: miscible 1000 g/L at 20 °C

密度

1.012 g/mL at 25 °C (lit.)

SMILES字符串

NCCO

InChI

1S/C2H7NO/c3-1-2-4/h4H,1-3H2

InChI key

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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其他说明

This product has been replaced by 15014-ALDRICH | Ethanolamine, ≥99% | NH2CH2CH2OH

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

靶器官

Respiratory system

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 2

闪点(°F)

195.8 °F - Pensky-Martens closed cup

闪点(°C)

91 °C - Pensky-Martens closed cup

个人防护装备

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

法规信息

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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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Fast one-step synthesis of N-doped carbon dots by pyrolyzing ethanolamine.
Dong X, et al.
Journal of Material Chemistry C, 2(36), 7477-7481 (2014)
Fong-Fu Hsu et al.
Journal of the American Society for Mass Spectrometry, 13(5), 558-570 (2002-05-22)
Negative-ion electrospray ionization tandem quadrupole mass spectrometry provides a useful method for the structural characterization of ceramides. Fragment ions referring to the identities of the fatty acid substituent and of the long chain base of the molecules are readily available
Aqueous solvation and functionalization of weak-acid polyelectrolyte thin films.
Peez RF, et al.
Langmuir, 14(15), 4232-4237 (1998)
Cristina Mayor-Ruiz et al.
Nature chemical biology, 16(11), 1199-1207 (2020-08-05)
Targeted protein degradation is a new therapeutic modality based on drugs that destabilize proteins by inducing their proximity to E3 ubiquitin ligases. Of particular interest are molecular glues that can degrade otherwise unligandable proteins by orchestrating direct interactions between target
Surface reactions of brominated arenes as a model for the formation of chlorinated dibenzodioxins and-furans in incineration: inhibition by ethanolamine.
Lippert T, et al.
Environmental Science & Technology, 25(8), 1485-1489 (1991)

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