• British Pharmacopoeia Volume I & II
  • Monographs: Medicinal and Pharmaceutical Substances

Trichloroacetic Acid

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General Notices

(Ph. Eur. monograph 1967)

bp2013_v2_13_medicinal_and_pharmaceutical_substances_18 trichloroaceticacid_1_2012_70_cs.png


C2HCl3O2    163.4    76-03-9

Preparation

Trichloroacetic Acid Solution

Ph Eur

DEFINITION

2,2,2-Trichloroacetic acid.

Content

98.0 per cent to 100.5 per cent.

CHARACTERS
Appearance

White or almost white, crystalline mass or colourless crystals, very deliquescent.

Solubility

Very soluble in water, in alcohol and in methylene chloride.

IDENTIFICATION

First identification   A.

Second identification   B, C.

A. Infrared absorption spectrophotometry (2.2.24).

Comparison   Ph. Eur. reference spectrum of trichloroacetic acid.

B. To 0.5 mL of solution S (see Tests) add 2 mL of pyridine R and 5 mL of strong sodium hydroxide solution R. Shake vigorously and heat in a water-bath at 60-70 °C for 5 min. The upper layer shows an intense red colour.

C. Solution S is strongly acidic (2.2.4).

TESTS
Solution S

Dissolve 2.5 g in water R and dilute to 25 mL with the same solvent.

Appearance of solution

Solution S is clear (2.2.1) and not more intensely coloured than reference solution BY7 (2.2.2, Method II).

Chlorides (2.4.4)

Maximum 100 ppm.

Dilute 5 mL of solution S to 15 mL with water R. The solution complies with the limit test for chlorides.

Sulfated ash (2.4.14)

Maximum 0.1 per cent, determined on 1.0 g.

ASSAY

Dissolve 0.150 g in 20 mL of water R. Titrate with 0.1 M sodium hydroxide, determining the end-point potentiometrically (2.2.20).

1 mL of 0.1 M sodium hydroxide is equivalent to 16.34 mg of C2HCl3O2.

STORAGE

In an airtight container.

Ph Eur