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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

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

Derivatizing reagent for amino acids, dipeptides, and nucleotides.

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

Certificates of Analysis (COA)

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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
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
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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