ChemicalBook--->CAS DataBase List--->34004-36-9

34004-36-9

34004-36-9 Structure

34004-36-9 Structure
IdentificationBack Directory
[Name]

(2,3-dihydroxypropyl)trimethylammonium chloride
[CAS]

34004-36-9
[Synonyms]

Levocarnitine Impurity 26
(2,3-Dihydroxypropyl)trimethylammoniumchlorid
(2,3-dihydroxypropyl)trimethylammonium chloride
2,3-Dihydroxy-N,N,N-trimethylpropan-1-aminium chloride
(2,3-DIHYDROXYPROPYL)TRIMETHYLAMMONIUM CHLORIDE (DHPTAC)
1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride
1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride (1:1)
[EINECS(EC#)]

251-783-2
[Molecular Formula]

C6H16ClNO2
[MDL Number]

MFCD01668726
[MOL File]

34004-36-9.mol
[Molecular Weight]

169.65
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to off-white Solid
[Cosmetics Ingredients Functions]

HUMECTANT
[EPA Substance Registry System]

1-Propanaminium, 2,3-dihydroxy-N,N,N-trimethyl-, chloride (34004-36-9)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[TSCA ]

TSCA listed
Hazard InformationBack Directory
[Uses]

Dihydroxypropyltrimonium Chloride is a useful research chemical compound used in the synthesis??of 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
[5] Chemische Berichte, 1869, vol. 2, p. 187
Spectrum DetailBack Directory
[Spectrum Detail]

(2,3-dihydroxypropyl)trimethylammonium chloride(34004-36-9)1HNMR
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