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C40200

2-Chloroethylamine hydrochloride

Name: 2-Chloroethylamine hydrochloride
Brand: ALDRICH

99%

Synonym(s):

2-Aminoethyl chloride hydrochloride

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About This Item

Linear Formula:

ClCH₂CH₂NH₂ · HCl

CAS Number:

870-24-6

Molecular Weight:

115.99

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892570

EC Number:

212-793-2

Beilstein/REAXYS Number:

3590304

MDL number:

MFCD00012887

Assay:

99%

Form:

crystals

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Properties

Quality Level

200

assay

99%

form

crystals

mp

140-150 °C (lit.)

SMILES string

Cl.NCCCl

InChI

1S/C2H6ClN.ClH/c3-1-2-4;/h1-2,4H2;1H

InChI key

ONRREFWJTRBDRA-UHFFFAOYSA-N

Description

Application

2-Chloroethylamine hydrochloride is used:

in the preparation of novel Schiff base ligands, that can also be used to remove metal ions such as Co (II) and Ni (II) from contaminated water when immobilized on silica gels)
as a derivatizing reagent

Derivatizing reagent for amino acids, dipeptides, and nucleotides.

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pictograms

GHS08,GHS05

signalword

Danger

hcodes

H290,H314,H341

pcodes

P202 - P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Muta. 2 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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In the search for new anticancer drugs. XXIV: Synthesis and anticancer activity of amino acids and dipeptides containing the 2-chloroethyl- and [N'-(2-chloroethyl)-N'-nitroso]-aminocarbonyl groups.

G Sosnovsky et al.

Journal of pharmaceutical sciences, 82(1), 1-10 (1993-01-01)

A series of L,L- (42, 44, 46, and 60) and D,D- (43, 45, 47, and 61) dipeptide derivatives composed of phenylglycine, phenylalanine, homophenylalanine, and valine and containing a 2-chloroethylamino group at the C-terminus and an N'-(2-chloroethyl)-N'-nitroso-aminocarbonyl group at the N-terminus

Synthesis of a carboxamide linked T*T dimer and its incorporation in oligonucleotides.

A Chur et al.

Nucleic acids research, 21(22), 5179-5183 (1993-11-11)

The condensation of 5'-O-protected 3'-O-(2-aminoethyl)thymidine with 1,2-dideoxy-1-thyminyl-beta-D-erythro-pentofuranuronic acid gives a T*T dimer with * representing a 3'-OCH2CH2NHC(O)-4' linkage connecting the two pentofuranosyl moieties. The incorporation of this dimer in oligonucleotide sequences show only moderately lowered Tm values when hybridized with

Peptide Cross-Linked Poly(2-oxazoline) as a Sensor Material for the Detection of Proteases with a Quartz Crystal Microbalance.

Norlaily Ahmad et al.

Biomacromolecules, 20(7), 2506-2514 (2019-06-28)

Inflammatory conditions are frequently accompanied by increased levels of active proteases, and there is rising interest in methods for their detection to monitor inflammation in a point of care setting. In this work, new sensor materials for disposable single-step protease

Global Trade Item Number

SKU	GTIN
C40200-100G	04061833486825
C40200-5G	04061833486832