(2,3-dihydroxypropyl)trimethylammonium chloride

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(2,3-dihydroxypropyl)trimethylammonium chloride Basic information
Product Name:(2,3-dihydroxypropyl)trimethylammonium chloride
Synonyms:(2,3-dihydroxypropyl)trimethylammonium chloride;1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride;(2,3-DIHYDROXYPROPYL)TRIMETHYLAMMONIUM CHLORIDE (DHPTAC) ;1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride (1:1);Levocarnitine Impurity 26;(2,3-Dihydroxypropyl)trimethylammoniumchlorid;N-[(2,3-dihydroxy)prop-1-yl]-N,N,N-trimethylammonium chloride;Levocarnitine Impurity 10 Chloride
CAS:34004-36-9
MF:C6H16ClNO2
MW:169.64974
EINECS:251-783-2
Product Categories:
Mol File:34004-36-9.mol
(2,3-dihydroxypropyl)trimethylammonium chloride Structure
(2,3-dihydroxypropyl)trimethylammonium chloride Chemical Properties
storage temp. Inert atmosphere,Room Temperature
AppearanceWhite to off-white Solid
Cosmetics Ingredients FunctionsHUMECTANT
EPA Substance Registry System1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride (34004-36-9)
Safety Information
TSCA TSCA listed
MSDS Information
(2,3-dihydroxypropyl)trimethylammonium chloride Usage And Synthesis
UsesDihydroxypropyltrimonium Chloride is a useful research chemical compound used in the synthesisof amine-functionalized branched polyethyleneimines with specific adhesion properties for surface modification.
Synthesis
3-Chloro-1,2-propanediol

96-24-2

Trimethylamine

75-50-3

(2,3-dihydroxypropyl)trimethylammonium chloride

34004-36-9

General procedure for the synthesis of 2,3-dihydroxypropyl-trimethylammonium chloride from 3-chloro-1,2-propanediol and trimethylamine: 0.00 g (±)-3-chloro-1,2-propanediol (0.452 mol), 178.00 g of a 30% aqueous solution of trimethylamine (0.904 mol), and 50 mL of deionized water were added to a 500 mL three-neck flask. Subsequently, the reaction system was warmed to 90 °C and stirred continuously at this temperature for 16 hours to ensure complete reaction of 3-chloro-1,2-propanediol. Upon completion of the reaction, the reaction mixture was cooled to 20 °C and extracted three times with ethyl acetate (100 mL x 3) to remove organic impurities. The aqueous phase was collected and concentrated to dryness by rotary evaporator to give 70.00 g of white solid product in 91.2% yield and 93.40% purity by HPLC.

References[1] Patent: CN108129338, 2018, A. Location in patent: Paragraph 0027; 0029; 0030
[2] Annales de Chimie (Cachan, France), 1879, vol. <5> 17, p. 114
[3] Chemische Berichte, 1869, vol. 2, p. 187
[4] Justus Liebigs Annalen der Chemie, 1904, vol. 337, p. 102
(2,3-dihydroxypropyl)trimethylammonium chloride Preparation Products And Raw materials
Raw materialsTrimethylamine-->3-Chloro-1,2-propanediol-->Trimethylamine hydrochloride-->2-Chloroethanol-->Glycidol
Tag:(2,3-dihydroxypropyl)trimethylammonium chloride(34004-36-9) Related Product Information
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