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Bismuth Subgallate Manufacturer Exporter BP Ph Eur USP Grade Manufacturer Exporter

Crystal Clear Products is a manufacturer exporter company manufacturing several chemicals including Bismuth Subgallate and IP BP Ph Eur USP NF JP ACS AR Analytical Reagent FCC Food Grade, Pharmaceutical Chemicals at best prices. The group has offices and factories in India USA and UAE and toll manufacturers in China and sells to almost every country in the world.

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Hazard Statements:
Not a hazardous substance or mixture according to Regulation (EC) No. 1272/2008.
This substance is not classified as dangerous according to Directive 67/548/EEC.
Not considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200)
Signal Word: None

Transport Information
DOT USA, TDG Canada & ADR/RID Europe: Not dangerous goods.
IMO/IMDG: Not dangerous goods.
IATA/ICAO: Not dangerous goods.

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Bismuth Subgallate SDS of Manufacturers

Bismuth Subgallate IP BP Ph Eur USP NF FCC Food AR ACS Reagenr Grade Manufacturers

CAS Number 99-26-3 Bismuth Subgallate, EINECS: 202-742-2, Molecular Weight: 394.09, Chemical Formula: C7H5BiO6

Bismuth Subgallate USP Grade Specifications
C7H5BiO6 -- 394.09
Gallic acid bismuth basic salt CAS 99-26-3

Bismuth Subgallate is a basic salt which, when dried at 105 for 3 hours, contains the equivalent of not less than 52.0 percent and not more than 57.0 percent of Bi2O3.

Identification:
A: When heated to redness, it at first chars, leaving finally a yellow residue. This residue responds to the tests for Bismuth.
B: Agitate thoroughly about 100 mg with an excess of hydrogen sulfide, filter, and boil the filtrate to expel the dissolved gas. Cool, and add 1 drop of ferric chloride: a purplish blue mixture is produced.
Loss on drying: Dry it at 105 for 3 hours. It loses not more than 7.0% of its weight.
Limit of nitrate: Mix about 100 mg with 5 mL of 2 N sulfuric acid and 5 mL of ferrous sulfate, filter the mixture, and carefully superimpose the filtrate, without mixing, on 5 mL of sulfuric acid, in a test tube: no reddish brown color appears at the zone of contact of the two liquids.
Arsenic: Triturate 400 mg with an equal weight of calcium hydroxide, and ignite. Dissolve the residue in 5 mL of 3 N hydrochloric acid: the solution without further treatment meets the requirements of the test for Arsenic 211 (7.5 ppm).
Copper, Lead, and Silver: To pass the test.
Limit of alkalies and alkaline earths: Boil 1.0 g with 20 mL of a mixture of equal volumes of 6 N acetic acid and water, cool, and filter. Precipitate the bismuth from the filtrate by the addition of hydrogen sulfide, boil the mixture, and filter. Add 5 drops of sulfuric acid to the filtrate, evaporate to dryness, and ignite to constant weight: the weight of the residue does not exceed 5 mg (0.5%).
Free gallic acid: Shake 1.0 g with 20 mL of alcohol for 1 minute, filter and evaporate the filtrate to dryness on a steam bath, and dry the residue at 105 for 1 hour: the weight of the residue does not exceed 5 mg (0.5%).

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Bismuth Subgallate BP Ph Eur Grade Specifications
C7H5BiO6
394.1 -- CAS 149-91-7
Ph Eur

DEFINITION
Complex of bismuth and gallic acid.
Content: 48.0 per cent to 51.0 per cent of Bi (Ar 209.0) (dried substance).

CHARACTERS
Appearance: Yellow powder.
Solubility: Practically insoluble in water and in alcohol. It dissolves in mineral acids with decomposition and in solutions of alkali hydroxides, producing a reddish-brown liquid.

IDENTIFICATION
A. Mix 0.1 g with 5 ml of water R and 0.1 ml of phosphoric acid R. Heat to boiling and maintain boiling for 2 min. Cool and filter. To the filtrate, add 1.5 ml of ferric chloride solution, a blackish-blue colour develops.
B. It gives reaction (b) of bismuth (2.3.1).

TESTS
Solution S: In a porcelain or quartz dish, ignite 1.0 g, increasing the temperature very gradually. Heat in a muffle furnace at 600 ± 50C for 2 h. Cool and dissolve the residue with warming in 4 ml of a mixture of equal volumes of lead-free nitric acid and water and dilute to 20 ml with water.
Acidity: Shake 1.0 g with 20 ml of water R for 1 min and filter. To the filtrate add 0.1 ml of methyl red solution. Not more than 0.15 ml of 0.1 M sodium hydroxide is required to change the colour of the indicator to yellow.
Chlorides: Maximum 200 ppm.
Nitrates: Maximum 0.2 per cent.
Copper: Maximum 50.0 ppm.
Lead: Maximum 20.0 ppm.
Silver: Maximum 25.0 ppm.
Substances not precipitated by ammonia: Maximum 1.0 per cent.
Loss on drying: Maximum 7.0 per cent, determined on 1.000 g by drying in an oven at 105C for 3 h.

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Last updated 11/19/2022

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