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C40200

Sigma-Aldrich

2-Chloroethylamine hydrochloride

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
Beilstein:
3590304
EC Number:
212-793-2
MDL number:
MFCD00012887
UNSPSC Code:
12352100
PubChem Substance ID:
24892570
NACRES:
NA.22
Pricing and availability is not currently available.

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

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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) [1]
  • as a derivatizing reagent [2]
Derivatizing reagent for amino acids,[3] dipeptides,[3] and nucleotides.[4]

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H290,H314,H341

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF3792V
WXBF3303V
WXBF3635V
WXBD6925V
WXBD5971V

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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
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
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

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