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Merck
CN

348287

(3-Chloro-2-hydroxypropyl)trimethylammonium chloride solution

60 wt. % in H2O, liquid

Synonym(s):

3-chloro-2-hydroxy-propyltrimethylammonium chloride

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About This Item

Linear Formula:
ClCH2CH(OH)CH2N(Cl)(CH3)3
CAS Number:
3327-22-8
Molecular Weight:
188.10
NACRES:
NA.22
PubChem Substance ID:
24861561
UNSPSC Code:
12352101
MDL number:
MFCD00055655
Beilstein/REAXYS Number:
6576172

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Product Name

(3-Chloro-2-hydroxypropyl)trimethylammonium chloride solution, 60 wt. % in H2O

InChI

1S/C6H15ClNO.ClH/c1-8(2,3)5-6(9)4-7;/h6,9H,4-5H2,1-3H3;1H/q+1;/p-1

SMILES string

[Cl-].C[N+](C)(C)CC(O)CCl

InChI key

CSPHGSFZFWKVDL-UHFFFAOYSA-M

form

liquid

concentration

60 wt. % in H2O

refractive index

n20/D 1.4541

density

1.154 g/mL at 25 °C

Quality Level

200

Related Categories

Application

(3-Chloro-2-hydroxypropyl)trimethylammonium chloride solution (CHTAC) can be used:
  • As a cation-generating agent for cellulose cationization by exhaustion method.
  • To resolve 2,2′-dihydroxy-1,1′-binaphthyl enantiomers.
  • To synthesize cationic glycogen (Cat Gly).
  • As a quaternizing agent for quaternization of N-aryl chitosan derivatives.

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H351,H412

Hazard Classifications

Aquatic Chronic 3 - Carc. 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN3058
BCCM6969
BCCK5690
BCCJ6319
BCCG5463

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Reaction efficiency for cellulose cationization using 3-chloro-2-hydroxypropyl trimethyl ammonium chloride
Hashem M, et al.
Textile Res., 73(11), 1017-1023 (2003)
Effect of cationization on adsorption of silver nanoparticles on cotton surfaces and its antibacterial activity
Khalil-Abad M, et al.
Cellulose, 16(6), 1147-1147 (2009)
Quaternization of N-aryl chitosan derivatives: synthesis, characterization, and antibacterial activity
Sajomsang W, et al.
Carbohydrate Research, 344(18), 2502-2511 (2009)
Deepak Sharma et al.
Carbohydrate polymers, 232, 115731-115731 (2020-01-19)
Galactomannans are branched natural biopolymers possessing good biocompatibility, biodegradability and sustainability leading to diverse industrial applications. In the present study, quaternization of galactomannan derived from Cassia tora gum was investigated by adopting Taguchi's approach of robust design of experiments using
Efficient resolution of 2, 2′-dihydroxy-1, 1′-binaphthyl by inclusion complexation with chiral N-(3-chloro-2-hydroxypropyl)-N, N, N-trimethylammonium chloride
Toda F, et al.
Organic & Biomolecular Chemistry, 2(4), 449-451 (2004)
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