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103-83-3

  • Product Name:N,N-Dimethylbenzylamine
  • Molecular Formula:C9H13N
  • Molecular Weight:135.209
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Product Details

Detail

  • Cas No: 103-83-3
  • Molecular Formula: C9H13N
  • Appearance: Colourless to light yellow liquid
  • Purity: 99%
Product Name N, N-dimethylbenzamine
Alias dimethylbenzylamine;N,N-Dimethylbenzylam;N-BENZYLDIETHYLAMINE
English
Molecular formula C9H13N
Molecular weight 135.21
CAS No 103-83-3
EINECS
Specification

Content > 99%

Water < 0.5%

Colour and lustre is < 100 # (APHA)

Appearance traits

properties: it is colorless to light yellow transparent liquid at normal temperature and has a strong ammonia flavor.

Use N, N - dimethyl benzylamine is a standard lumbar soft bubble and hard foaming catalyst, as well as organic synthesis and acid neutralizing agent and dehydrogenation catalyst.
Package 180 kg/barrels or according to customer requirements
Other product information

Density 0.9;

Melting point - 75 oC;

Boiling point 183-184 oC;

Refractive index 1.5-1.502;

Flash point 54 oC;

Water soluble 8 g/L (20 oC);

Factory supply N,N-Dimethylbenzylamine 103-83-3 (N-(Phenylmethyl)dimethylamine)  with low price

  • Molecular Formula:C9H13N
  • Molecular Weight:135.209
  • Appearance/Colour:Colourless to light yellow liquid 
  • Vapor Pressure:0.871mmHg at 25°C 
  • Melting Point:-75 °C 
  • Refractive Index:n20/D 1.501(lit.)  
  • Boiling Point:181 °C at 760 mmHg 
  • PKA:pK1:9.02(+1) (25°C) 
  • Flash Point:130 °F 
  • PSA:3.24000 
  • Density:0.9 g/mL at 25 °C(lit.) 
  • LogP:1.74820 

N,N-Dimethylbenzylamine(Cas 103-83-3) Usage

Preparation

25% Aqueous Dimethylamine, 1088 grams Benzyl Chloride, 126.6 grams In the apparatus of Example 1, the benzyl chloride was added dropwise over a two-hour period to the amine (molar ratio 1 to 6) at a rate sufficient to maintain the temperature below 40°C. Stirring was continued at room temperature for an additional hour to insure completion of the reaction denoted by the equation below. Thereafter the reaction mixture was cooled in a separatory funnel while standing in a refrigerator maintained at 5° C. and separated into two layers. The upper oily layer, weighing 111.5g, was removed and steam distilled until no further oleaginous component was observed in the distillate as it came over. The crude distillate was found to contain 103.5g of N,N-dimethylbenzylamine (76.1% of theory), 3.3g of dimethylamine and no quaternary salts. The dimethylamine was distilled off below 29°C under atmospheric pressure from the N,N-dimethylbenzylamine (bp 82°C/18mmHg).

Synthesis Reference(s)

The Journal of Organic Chemistry, 40, p. 531, 1975 DOI: 10.1021/jo00892a043Synthetic Communications, 6, p. 539, 1976 DOI: 10.1080/00397917608063545

Air & Water Reactions

Flammable. Slightly soluble in water.

Reactivity Profile

N,N-Dimethylbenzylamine neutralizes acids on exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. May attack some plastics [USCG, 1999].

Health Hazard

Inhalation may be fatal as a result of spasm, inflammation and edema of the larynx and bronchi, chemical pneumonitis, and pulmonary edema. Symptoms of exposure may include burning sensation, coughing, wheezing, laryngitis, shortness of breath, headache, nausea, and vomitting.

Fire Hazard

Special Hazards of Combustion Products: Toxic vapors are generated when heated.

Flammability and Explosibility

Flammable

Safety Profile

Poison by ingestion. Moderately toxic by inhalation and skin contact. Corrosive. A severe eye and skin irritant. Flammable when exposed to heat or flame. When heated to decomposition it emits toxic fumes of NOx

Purification Methods

Dry the amine over KOH pellets and fractionate it over Zn dust in a CO2—free atmosphere. It has a pKa2 5 of 8.25 in 45% aqueous EtOH. Store it under N2 or in a vacuum. The picrate has m 94-95o, and the picrolonate has m 151o (from EtOH). [Skita & Keil Chem Ber 63 34 1930, Coleman J Am Chem Soc 55 3001 1933, Devereux et al. J Chem Soc 2845 1957.] The tetraphenyl borate salt has m 182-185o. [Crane Anal Chem 28 1794 1956, Beilstein 12 IV 2161.]

General Description

A colorless to light yellow liquid with an aromatic odor. Slightly less dense than water and slightly soluble in water. Flash point approximately 140°F. Corrosive to skin, eyes and mucous membranes. Slightly toxic by ingestion, skin absorption and inhalation. Used in the manufacture of adhesives and other chemicals.

InChI:InChI=1/C9H13N/c1-10(2)8-9-6-4-3-5-7-9/h3-7H,8H2,1-2H3/p+1

Our main markets are China, the United States, Europe, Korea, and Japan. The main business scope includes electronic chemicals, liquid crystal intermediates, high-purity metal compounds, pharmaceutical intermediates, special chemicals, and so on.

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103-83-3 Process route

2-chloro-benzaldehyde
89-98-5

2-chloro-benzaldehyde

dimethyl amine
124-40-3

dimethyl amine

N,N'-dimethylbenzylamine
103-83-3

N,N'-dimethylbenzylamine

2-Chlorobenzyl alcohol
17849-38-6

2-Chlorobenzyl alcohol

1-(2-chlorophenyl)-N,N-dimethylmethanamine
10175-31-2

1-(2-chlorophenyl)-N,N-dimethylmethanamine

Conditions
Conditions Yield
With acetic acid; In water; at 99.84 ℃; for 3h; under 3750.38 Torr; Inert atmosphere;
 
N,N-dimethylthiobenzamide
15482-60-7

N,N-dimethylthiobenzamide

N,N'-dimethylbenzylamine
103-83-3

N,N'-dimethylbenzylamine

dibenzyl disulphide
150-60-7

dibenzyl disulphide

phenylmethanethiol
100-53-8

phenylmethanethiol

Conditions
Conditions Yield
With sodium tetrahydroborate; In acetonitrile; for 26h; Heating;
6%
23%
63%

103-83-3 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 64-18-6
    64-18-6

    formic acid

  • 706-03-6
    706-03-6

    3-(benzylamino)propionitrile

  • 5400-93-1
    5400-93-1

    1-benzyl-3,5,7-triaza-1-azoniatricyclo<3,3,1,13,7>decane chloride

103-83-3 Downstream products

  • 120-51-4
    120-51-4

    benzoic acid benzyl ester

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    84555-07-7

    benzyl-butoxycarbonylmethyl-dimethyl-ammonium; chloride

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    5467-99-2

    4-methylbenzoic acid benzyl ester

  • 120383-72-4
    120383-72-4

    benzyl-dimethyl-phenoxycarbonylmethyl-ammonium; chloride

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