Bismuth Subgallate N Bismuth Subsalicylate Manufacturer Exporter

Annie Chemie P Ltd, is a company at Dahej in Gujarat, India. It is a manufacturer exporter of Bismuth Subgallate & Bismuth Subsalicylate and oil field shale gas fracking or hydraulic fracturing chemicals and speciality chemicals and it has substantial exports to countries like USA, Canada, UK, Europe, UAE, Nigeria, Algeria, Turkey, Mexico, Brazil, Chile, Argentina, Australia, Kuwait, Dubai etc. We have developed encapsulated guar gel breaker based on coated ammonium persulfate, potassium persulfate, sodium persulfate, potassium peroxymonopersulfate, sodium bromate etc. We also supply other coated or encapsulated products like citric acid, guar crosslinkers other shale gas frac related products like diverting agent, KCl-substitute or clay-stabilizer, corossion inhibitors, scale inhibitor, bio-guard and several speciality chemicals.

Bismuth Subgallate USP BP Ph Eur Grade & Bismuth Subsalicylate USP BP Ph Eur Grade Suppliers Exporters, Manufacturers

Bismuth Subgallate
CAS Number: 99-26-3 or 149-91-7 USP BP Ph Eur Grade Suppliers Exporters, Manufacturers
Bismuth Subgallate Manufacturers Exporters

Bismuth Subgallate Manufacturers Exporters

Specifications of Bismuth Subgallate USP Grade
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%).

Specifications of Bismuth Subgallate BP Ph Eur Grade
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.

Bismuth Subsalicylate
CAS Number: 14882-18-9 USP BP Ph Eur Grade Suppliers Exporters, Manufacturers
Bismuth Subsalicylate Manufacturers Exporters

Bismuth Subsalicylate Manufacturers Exporters

Bismuth Subsalicylate USP Grade Specifications
C7H5BiO4 -- 362.09
(2-Hydroxybenzoato-O1)-oxobismuth.
2-Hydroxybenzoic acid bismuth (3+) salt, basic CAS 14882-18-9.

Bismuth Subsalicylate is a basic salt that when dried at 105 for 3 hours contains not less than 56.0 percent and not more than 59.4 percent of bismuth (Bi) and not less than 36.5 percent and not more than 39.3 percent of total salicylates.

Identification:
A: Infrared Absorption.
B: It responds to the tests for Bismuth.
pH: between 2.7 and 5.0, in a solution prepared as follows. Mix 10 g of Bismuth Subsalicylate and 90 mL of water, shake by mechanical means for 10 minutes, and filter.
Loss on drying: Dry it at 105C for 3 hours: it loses not more than 1.0% of its weight.
Limit of nitrate: 0.4%.
Arsenic: The limit is 10 µg per g.
Limit of free salicylic acid: To pass the test. (Not more than 0.2%).
Limit of copper, lead, and silver: To pass the test. (40 µg per g).

Bismuth Subsalicylate BP Ph Eur Grade Specifications
C7H5BiO4
362.1 -- CAS 14882-18-9

DEFINITION
Complex of bismuth and salicylic acid.
Content: 56.0 per cent to 59.4 per cent of Bi (Ar 209.0) (dried substance).

CHARACTERS
Appearance: White or almost white powder.
Solubility: Practically insoluble in water and in alcohol. It dissolves in mineral acids with decomposition.

IDENTIFICATION
A. To 0.5 g add 10 ml of hydrochloric acid. Heat on a boiling water-bath for 5 min. Cool and filter. Retain the filtrate for identification test B. Wash the residue with dilute hydrochloric acid and then with water. Dissolve the residue in 0.5-1 ml of dilute sodium hydroxide solution. Add 15 ml of water. Neutralise with dilute hydrochloric acid. The solution gives reaction (a) of salicylates.
B. The filtrate obtained in identification test A gives reaction (b) of bismuth.

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 ± 25C 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 2.0 g with 30 ml of ether for 1 min and filter. To the filtrate add 30 ml of alcohol and 0.1 ml of thymol blue solution. Not more than 0.35 ml of 0.1 M sodium hydroxide is required to change the colour of the indicator to blue.
Chlorides: Maximum 200 ppm.
Nitrates: Maximum 0.4 per cent.
Copper: Maximum 50.0 ppm.
Lead: Maximum 20.0 ppm.
Silver: Maximum 25.0 ppm.
Soluble bismuth: Maximum 40.0 ppm.
Loss on drying: Maximum 1.0 per cent, determined on 1.000 g by drying in an oven at 105C.

Bismuth Subgallate CAS Number 99-26-3 or 149-91-7 & Bismuth Subsalicylate CAS Number 14882-18-9 Supplier Exporter, Manufacturer:

Annie Chemie P Ltd
Mumbai 4000010, INDIA
With Agents and offices in UAE, USA, Europe.

Exporters to USA, Canada, UK, Europe, UAE, Nigeria, Algeria, Turkey, Mexico, Brazil, Chile, Argentina, Australia, Dubai etc.