23035
2-Chloroethylamine hydrochloride
purum, ≥98.0% (AT)
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
Recommended Products
grade
purum
Quality Level
Assay
≥98.0% (AT)
form
solid
mp
140-150 °C (lit.)
140-150 °C
functional group
amine
chloro
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 can be used in the preparation of novel Schiff base ligands. These ligands, when immobilized on silica gels, form inexpensive materials for the removal of metal ions such as Ni2+ and Co2+ ions from contaminated water.
Other applications:
Other applications:
- Alginate derivatization via aminoethylation to form aminoethyl alginate.
- Synthesis of N-(2-chloroethyl)-benzaldimine.
- Derivatization of starch to form aminoethyl (AE-St) starch derivatives.
Signal Word
Danger
Hazard Statements
Precautionary Statements
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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Preparation of polypropylene based hyperbranched absorbent fibers and the study of their adsorption of CO2
Xu T, et al.
Royal Society of Chemistry Advances, 5(42), 32902-32908 (2015)
Production of L (+) lactic acid by Lactobacillus delbrueckii immobilized in functionalized alginate matrices.
Rao C S, et al.
World Journal of Microbiology & Biotechnology, 24(8), 1411-1415 (2008)
Chemical modification of silica gel with synthesized new Schiff base derivatives and sorption studies of cobalt (II) and nickel (II).
Kursunlu A N, et al.
Applied Surface Science, 255(21), 8798-8803 (2009)
Joachim F R Van Guyse et al.
Polymers, 13(3) (2021-02-04)
Smart or adaptive materials often utilize stimuli-responsive polymers, which undergo a phase transition in response to a given stimulus. So far, various stimuli have been used to enable the modulation of drug release profiles, cell-interactive behavior, and optical and mechanical
Khalil Sakeer et al.
Carbohydrate polymers, 163, 108-117 (2017-03-08)
Different starch derivatives were evaluated as supports for attachment and recovery of macrophages (RAW 264.7 line). Gelatinized starch (G-St), acetate starch (Ac-St), carboxymethyl starch and aminoethyl starch were synthesized and characterized by FTIR, 1H NMR, SEM and static water contact
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