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Merck
CN

D87201

2-Chloro-N,N-diethylethylamine hydrochloride

99%

Synonym(s):

2-(Diethylamino)ethyl chloride hydrochloride, 2-Chlorotriethylamine hydrochloride

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About This Item

Linear Formula:
(C2H5)2NCH2CH2Cl · HCl
CAS Number:
869-24-9
Molecular Weight:
172.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894220
EC Number:
212-786-4
Beilstein/REAXYS Number:
3591991
MDL number:
MFCD00012519
Assay:
99%
Form:
crystals

Key Documents

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InChI key

RAGSWDIQBBZLLL-UHFFFAOYSA-N

InChI

1S/C6H14ClN.ClH/c1-3-8(4-2)6-5-7;/h3-6H2,1-2H3;1H

SMILES string

Cl.CCN(CC)CCCl

assay

99%

form

crystals

mp

208-210 °C (lit.)

Quality Level

200

Related Categories

Application

2-Chloro-N,N-diethylethylamine hydrochloride can be used as an alkylating reagent for the synthesis of:
  • Substituted oxindole derivatives to be used as growth hormone secretagogs.
  • 1-Substituted-5,6-dinitrobenzimidazoles with antimicrobial and antiprotozoal activities.
  • Thiophene containing triarylmethane (TRAM) derivatives to be used as antitubercular agents.
  • Tris(2-(diethylamino)ethyl)amine to be used as a catalyst in combination with CuBr (Et6TREN/CuBr) for atom transfer radical polymerization of n-butyl acrylate.

It can also be used for the derivatization of chitosan to incorporate aminofunctionality onto it at C-6 position.

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Danger

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

Regulatory Information

监管及禁止进口产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN3993
BCCL7811
BCCL7812
BCCK2249
BCCK2248

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New amine-based tripodal copper catalysts for atom transfer radical polymerization.
Inoue Y and Matyjaszewski K
Macromolecules, 37(11), 4014-4021 (2004)
Thiophene containing triarylmethanes as antitubercular agents.
Parai MK, et al.
Bioorganic & Medicinal Chemistry Letters, 18(1), 289-292 (2008)
Reactive oxygen species scavenging activity of aminoderivatized chitosan with different degree of deacetylation.
Je JY, et al.
Bioorganic & Medicinal Chemistry, 14(17), 5989-5994 (2006)
Oxindole derivatives as orally active potent growth hormone secretagogues.
Tokunaga T, et al.
Journal of medicinal chemistry, 44(26), 4641-4649 (2001)
Ahmed M Omer et al.
Molecules (Basel, Switzerland), 26(2) (2021-01-21)
An effective drug nanocarrier was developed on the basis of a quaternized aminated chitosan (Q-AmCs) derivative for the efficient encapsulation and slow release of the curcumin (Cur)-drug. A simple ionic gelation method was conducted to formulate Q-AmCs nanoparticles (NPs), using
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