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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:
Molecular Weight:
115.99
Beilstein:
3590304
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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Related Categories

Application

Derivatizing reagent for amino acids, dipeptides, and nucleotides.

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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