N-Hexadecyltrimethylammonium chloride

Basic information

  • Product Name:N-Hexadecyltrimethylammonium chloride
  • CasNo.:112-02-7
  • MF:C19H42N.Cl
  • MW:320.002

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:232-234 °C
  • Packing:White or yellowish paste or solid
  • Throughput:
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Product Details

CasNo: 112-02-7

MF: C19H42N.Cl

Appearance: White or yellowish paste or solid

Reliable Quality Factory Supply 112-02-7 Cetyl Trimethyl Ammonium Chloride with Fast Delivery

  • Molecular Formula:C19H42N.Cl
  • Molecular Weight:320.002
  • Appearance/Colour:White or yellowish paste or solid 
  • Vapor Pressure:0.006Pa at 25℃ 
  • Melting Point:232-234 °C 
  • Refractive Index:n20/D 1.3778  
  • Boiling Point:100oC 
  • PSA:0.00000 
  • Density:0.968 g/mL at 25 °C 
  • LogP:3.17790 

N-Hexadecyltrimethylammonium chloride(Cas 112-02-7) Usage

Definition

ChEBI: The organic chloride salt of cetyltrimethylammonium.

General Description

Colorless to pale yellow liquid with an odor of rubbing alcohol. Floats or sinks in water.

Reactivity Profile

Acidic salts, such as N-Hexadecyltrimethylammonium chloride, are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.

Hazard

A poison by ingestion and skin contact.

Health Hazard

Ingestion may produce toxic effects. Contact with eyes or skin may cause severe damage.

Flammability and Explosibility

Nonflammable

Purification Methods

Crystallise the chloride from acetone/ether mixture, EtOH/ether, or from MeOH. [Moss et al. J Am Chem Soc 109 4363 1987, Beilstein 4 IV 819.]

InChI:InChI:1S/C19H42N.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(2,3)4;/h5-19H2,1-4H3;1H/q+1;/p-1

112-02-7 Relevant articles

The Pseudophase Model of Micellar Catalysis. Addition of Cyanide Ion to N-Alkylpyridinium Ions

Bunton, Clifford A.,Romsted, Laurence S.,Thamavit, Chirasarit

, p. 3900 - 3903 (1980)

Cationic micelles speed addition of cyan...

-

Hauser,Niles

, p. 954,958 (1941)

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STABLE COMPOSITIONS OF THIABENDAZOLE AND IODINE-CONTAINING FUNGICIDES

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, (2015/02/25)

The present invention relates to stable ...

FUNGICIDAL PENFLUFEN MIXTURES

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, (2014/04/03)

The invention relates to mixtures compri...

ACTIVE DELIVERY SYSTEMS FORMULATIONS

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, (2010/03/04)

The present invention relates to active ...

DENTAL ORAL COMPOSITION

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, (2010/11/03)

A dental composition for oral use, conta...

112-02-7 Process route

methylene chloride
74-87-3

methylene chloride

N,N-dimethylhexadecylamine
112-69-6

N,N-dimethylhexadecylamine

cetyltrimethylammonium chloride
112-02-7,79728-63-5

cetyltrimethylammonium chloride

Conditions
Conditions Yield
With Petroleum ether; at 80 ℃;
 
1-Chlorohexadecan
4860-03-1

1-Chlorohexadecan

trimethylamine
75-50-3

trimethylamine

cetyltrimethylammonium chloride
112-02-7,79728-63-5

cetyltrimethylammonium chloride

Conditions
Conditions Yield
With ethanol; at 100 - 105 ℃;
 
In isopropyl alcohol; for 72h; Heating;
 

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