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Merck
CN

A55209

Sigma-Aldrich

1-(2-氨乙基)哌嗪

99%

别名:

2-(1-哌嗪基)乙胺

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关于此项目

经验公式(希尔记法):
C6H15N3
CAS Number:
分子量:
129.20
Beilstein:
104363
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度

4.4 (vs air)

质量水平

蒸汽压

0.05 mmHg ( 20 °C)

方案

99%

表单

liquid

折射率

n20/D 1.5 (lit.)

沸点

218-222 °C (lit.)

密度

0.985 g/mL at 25 °C (lit.)

SMILES字符串

NCCN1CCNCC1

InChI

1S/C6H15N3/c7-1-4-9-5-2-8-3-6-9/h8H,1-7H2

InChI key

IMUDHTPIFIBORV-UHFFFAOYSA-N

应用

用于多种反应以研究缓蚀、生物活性 和催化金属配体效应

象形图

Skull and crossbonesCorrosion

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Skin Corr. 1B - Skin Sens. 1

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

闪点(°F)

197.6 °F - closed cup

闪点(°C)

92 °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

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Chao Lin et al.
Journal of controlled release : official journal of the Controlled Release Society, 116(2), 130-137 (2006-11-03)
A group of novel poly(amido amine) homo- and copolymers (PAAs) containing secondary and tertiary amine groups in their main chain and different structures in the bisacrylamide segments were synthesized and evaluated as non-viral gene delivery vectors. Among these, also the
J. Chem. Soc. Perkin Trans. II, 939-939 (1992)
S M Sami et al.
Journal of medicinal chemistry, 36(6), 765-770 (1993-03-19)
A new class of antitumor agents, having structural analogy to amonafide, but differing by the addition of a fourth ring in the nucleus, was synthesized conveniently from anthracene. Compounds with a variety of substituents, containing a basic nitrogen atom and
Tetrahedron, 48, 1999-1999 (1992)
H W Leung
Mutation research, 320(1-2), 31-43 (1994-01-01)
A series of 6 alkyleneamines [ethylenediamine (EDA), diethylenetriamine (DETA), triethylenetetramine (TETA), tetraethylenepentamine (TEPA), aminoethylethanolamine (AEEA), and aminoethylpiperazine (AEP)] were evaluated for potential genotoxic activity using a battery of in vitro and in vivo assays. Only TETA was considered mutagenic in

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