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A55209

1-(2-Aminoethyl)piperazine

Name: 1-(2-Aminoethyl)piperazine
Brand: ALDRICH

99%

Synonym(s):

2-Piperazinoethylamine

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About This Item

Empirical Formula (Hill Notation):

C₆H₁₅N₃

CAS Number:

140-31-8

Molecular Weight:

129.20

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24890984

EC Number:

205-411-0

Beilstein/REAXYS Number:

104363

MDL number:

MFCD00005971

Assay:

99%

Form:

liquid

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Properties

vapor density

4.4 (vs air)

Quality Level

100

vapor pressure

0.05 mmHg ( 20 °C)

assay

99%

form

liquid

refractive index

n20/D 1.5 (lit.)

bp

218-222 °C (lit.)

density

0.985 g/mL at 25 °C (lit.)

SMILES string

NCCN1CCNCC1

InChI

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

InChI key

IMUDHTPIFIBORV-UHFFFAOYSA-N

Description

Application

Utilized in a variety of reactions for studying corrosion inhibition, biological activity, and metal ligand effects on catalysis.

pictograms

GHS06,GHS05

signalword

Danger

hcodes

H302,H311,H314,H317,H412

pcodes

P261 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

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

Storage Class

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

wgk

WGK 2

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Linear poly(amido amine)s with secondary and tertiary amino groups and variable amounts of disulfide linkages: synthesis and in vitro gene transfer properties.

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

2-substituted 1,2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones. A new class of antitumor agent.

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

J. Chem. Soc. Perkin Trans. II, 939-939 (1992)

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Global Trade Item Number

SKU	GTIN
A55209-100G	04061833375976
A55209-500G	04061833375983