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Hexadecyl 3-amino-4-chlorobenzoate

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Hexadecyl 3-amino-4-chlorobenzoate Basic information

Product Name:
Hexadecyl 3-amino-4-chlorobenzoate
Synonyms:
  • 3-AMINO-4-CHLORO BENZOIC ACID HEXADECYL ESTER
  • HEXADECYL 3-AMINO-4-CHLOROBENZOATE
  • 3-Amino-4-chloro benzoic hexadecyl ester
  • 3-AMINO-4-CHLOROBENZOICACIDHEXADECYLESTERAPPEARANCE
  • Hexadecylester, 3-Amino-4-chloro benzoate
  • 3-Amino-4-chlorobenzoic acid hexadecyl ester in stock Factory
  • Benzoic acid, 3-amino-4-chloro-, hexadecyl ester
CAS:
143269-74-3
MF:
C23H38ClNO2
MW:
396.01
EINECS:
419-700-6
Product Categories:
  • Organic acids
Mol File:
143269-74-3.mol
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Hexadecyl 3-amino-4-chlorobenzoate Chemical Properties

Boiling point:
495.5±25.0 °C(Predicted)
Density 
1.017±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
1.48±0.10(Predicted)
CAS DataBase Reference
143269-74-3(CAS DataBase Reference)
EPA Substance Registry System
Benzoic acid, 3-amino-4-chloro-, hexadecyl ester (143269-74-3)
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Safety Information

Hazard Codes 
N
Risk Statements 
51/53
Safety Statements 
61
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Hexadecyl 3-amino-4-chlorobenzoate Usage And Synthesis

Chemical Properties

White to light brown crystalline powder

Synthesis

A mixture of 16.3 g (0.132 moles) 45percent potassium hydroxide solution, 21.5 g (0.125 moles) of 3-amino-4-chlorobenzoic acid, 100 g of xylene, 40/3 g (0.132 moles) of 1-bromohexadecane and 4.5 g of benzyltriethylammonium bromide (10 mol percent) was heated to reflux. Water was removed using a Dean-Stark trap. After 3 hr at reflux (115-120° C.), the reaction was judged complete by tic. The reaction was cooled to 90° C. and washed with water to remove salts. The solvent was removed on a roto-vap, and the residue was crystallized from heptane to give 40.7 g (83 per cent yield) of a solid Hexadecyl 3-amino-4-chlorobenzoate.

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