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Ferrous Fumarate USP BP Ph Eur IP FCC Food Grade Manufacturers

Anmol Chemicals is a manufacturer supplier exporter of Ferrous Fumarate and it offers materials as per IP BP EP Ph Eur USP NF JP FCC Food Grade as per the the latest monograph at best prices. Anmol Chemicals Group, established in 1976, is the pioneer manufacturer of Specialty Chemicals, Pharmaceutical Excipients, Some API, Food Chemicals in India. Anmol Chemicals Group has manufacturing facilities spread across Western India, representatives in Houston, Chicago USA and Dubai, UAE. We also have toll manufacturing units for processing chemicals in a few countries around the world. We make IP, BP, EP, USP, NF, Ph. Eur., JP, FCC or Food Grade, Analytical Reagent Grade, LR or Laboratory Reagent Grades and Pure Grades of various chemicals. All our items are analyzed to meet the required standards. We can supply the product in grams for your laboratory trial and in tons for your plant scale jobs.

We manufacture Bulk Drugs / API, Excipients, Pharmaceuticals (IP BP USP NF Ph Eur EP JP), Specialty Chemicals (Pure/Reagent), Mineral Fortifiers (FCC). Our manufacturing facility is FDA approved and GLP, cGMP, ISO9001, ISO14001, ISO/IEC 17025, ISO22000, FSSC 22000, ISO45001, FSSAI, Kosher, HALAL, COPP, WHO-GMP certified and Written Confirmation (WC) is available. Solid materials can be customized for particle size, shape, and bulk density. We observe WHO Good Manufacturing Practices and Good Laboratory Practices. We are a government-recognized STAR Export House and "Authorised Economic Operator (AEO)" per Indian Customs.

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Ferrous Fumarate SDS of Manufacturers

Ferrous Fumarate Manufacturers

Synonyms: ----
CAS Number: 141-01-5, Molecular Weight: 169.9, Chemical Formula: C4H2FeO4, EINECS EC Number: 205-447-7, FEMA: ----,

Ferrous Fumarate BP Grade Ph Eur Grade Specifications
C4H2FeO4 --- 169.9 --- CAS 141-01-5

DEFINITION
Iron (II) (E)-butenedioate.
Content
93.0 per cent to 101.0 per cent (dried substance).

CHARACTERS
Appearance: Fine, reddish-orange or reddish-brown powder.
Solubility: Slightly soluble in water, very slightly soluble in ethanol (96 per cent).

IDENTIFICATION
A. Thin-layer chromatography.
B. Mix 0.5 g with 1 g of resorcinol R. To 0.5 g of the mixture in a crucible add 0.15 ml of sulphuric acid R and heat gently. A dark red semi-solid mass is formed. Add the mass, with care, to 100 ml of water R. An orange-yellow colour develops and the solution shows no fluorescence.
C. The filtrate obtained during preparation of the test solution in identification test A gives reaction (a) of iron (2.3.1).

TESTS
Solution S :Dissolve 2.0 g in a mixture of 10 ml of lead-free hydrochloric acid R and 80 ml of water R, heating slightly if necessary. Allow to cool, filter if necessary and dilute to 100 ml with water R.
Sulphates: Maximum 0.2 per cent.
Arsenic: Maximum 5 ppm.
Ferric ion: Maximum 2.0 per cent.
Cadmium: Maximum 10.0 ppm.
Chromium: Maximum 2.00 × 102 ppm.
Lead: Maximum 20.0 ppm.
Mercury: Maximum 1.0 ppm.
Nickel: Maximum 2.00 × 102 ppm.
Zinc: Maximum 5.00 × 102 ppm.
Loss on drying: Maximum 1.0 per cent, determined on 1.000 g by drying in an oven at 105C.


Ferrous Fumarate USP Grade Specifications
C4H2FeO4 --- 169.90
2-Butenedioic acid, (E)-, iron(2+) salt.
Iron(2+) fumarate [CAS 141-01-5].

Ferrous Fumarate contains not less than 97.0 percent and not more than 101.0 percent of C4H2FeO4, calculated on the dried basis.

Identification:
A: To 1.5 g add 25 mL of dilute hydrochloric acid (1 in 2). Dilute with water to 50 mL, heat to dissolve, then cool, filter on a fine-porosity, sintered-glass crucible, wash the precipitate with dilute hydrochloric acid (3 in 100), saving the filtrate for Identification test B, and dry the precipitate at 105C: the IR absorption of a potassium bromide dispersion of the dried precipitate so obtained exhibits maxima only at the same wavelengths as that of a similar preparation of USP Fumaric Acid RS.
B: A portion of the filtrate obtained in the preceding test responds to the tests for Iron.
Loss on drying: Dry it at 105C for 16 hours: it loses not more than 1.5% of its weight.
Sulfate: Transfer 1.0 g to a 250-mL beaker, add 100 mL of water, and heat on a steam bath, adding hydrochloric acid drop wise, until complete solution is effected (about 2 mL of the acid will be required). Filter the solution if necessary, and dilute the filtrate with water to 100 mL. Heat the filtrate to boiling, add 10 mL of barium chloride TS, warm on a steam bath for 2 hours, cover, and allow to stand for 16 hours. (If crystals of ferrous fumarate form, warm the solution on the steam bath to dissolve them.) Pass the solution through ash less filter paper, wash the residue with hot water until, with the addition of ammonium sulfide TS, a black precipitate is no longer formed in the filtrate, and transfer the paper containing the residue to a tared crucible. Char the paper, without burning, and ignite the crucible and its contents at 600 to constant weight: each mg of residue is equivalent to 0.412 mg of SO4. Not more than 0.2% is found.
Arsenic: Transfer 2.0 g to a beaker, and add 10 mL of water and 10 mL of sulfuric acid. Warm to precipitate the fumaric acid completely, cool, add 30 mL of water, and filter into a 100-
mL volumetric flask. Wash the precipitate with water, adding the washings to the flask, add water to volume, and mix. Transfer 50.0 mL of this solution into the arsine generator flask, and dilute with water to 55 mL: the resulting solution meets the requirements of the test, the addition of 20 mL of 7 N sulfuric acid specified for Procedure being omitted. The limit is 3 ppm.
Limit of ferric iron: Transfer 2.0 g, accurately weighed, to a glass-stoppered, 250-mL conical flask, add 25 mL of water and 4 mL of hydrochloric acid, and heat on a hot plate until solution is complete. Insert the stopper in the flask, and cool to room temperature. Add 3 g of potassium iodide, insert the stopper in the flask, swirl to mix, and allow to stand in the dark for 5 minutes. Remove the stopper, add 75 mL of water, and titrate with 0.1 N sodium thiosulfate VS, adding 3 mL of starch TS as the end-point is approached. Not more than 7.16 mL of 0.1 N sodium thiosulfate is consumed (2.0%).
Limit of lead: To pass the atomic absorption spectrophotometer test. The Test solution does not exceed that of the Standard solution (0.001%).
Mercury: To pass the test of 3 µg per g.
Assay— Transfer 500 mg of Ferrous Fumarate, accurately weighed, to a 500-mL conical flask, and add 25 mL of dilute hydrochloric acid (2 in 5). Heat to boiling, and add a solution of 5.6 g of stannous chloride in 50 mL of dilute hydrochloric acid (3 in 10) drop wise until the yellow color disappears, then add 2 drops in excess. Cool the solution in an ice bath to room temperature, add 10 mL of mercuric chloride solution (1 in 20), and allow to stand for 5 minutes. Add 200 mL of water, 25 mL of dilute sulfuric acid (1 in 2), and 4 mL of phosphoric acid, then add 2 drops of orthophenanthroline TS, and titrate with 0.1 N ceric sulfate VS. Perform a blank determination, and make any necessary correction. Each mL of 0.1 N ceric sulfate is equivalent to 16.99 mg of C4H2FeO4.


Ferrous Fumarate IP Grade


Ferrous Fumarate FCC Food Grade Specifications
Iron (II) Fumarate FCC
C4H2FeO4 --- Formula weight 169.90 --- CAS 141-01-5

DESCRIPTION
Ferrous Fumarate occurs as a red-orange to red-brown powder. It may contain soft lumps that produce a yellow streak when crushed. It is soluble in water and in alcohol.
Function: Nutrient.

REQUIREMENTS
Identification:
A. Add 25 mL of 1:2 hydrochloric acid to about 1.5 g of sample, and dilute to 50 mL with water. Heat to effect complete solution; then cool; filter on a fine-porosity, sintered glass crucible; wash the precipitate with 2:100 hydrochloric acid, saving the filtrate for Identification Test B; and dry the precipitate at 105C. Add 3 mL of water and 7 mL of 1 N sodium hydroxide to 400 mg of the dried precipitate, and stir until solution is complete. Add, drop wise, 2.7 N hydrochloric acid until the solution is just acid to litmus; add 1 g of pnitrobenzyl
bromide and 10 mL of alcohol; and reflux the mixture for 2 h. Cool, filter, and wash the precipitate with two small portions of a 2:1 alcohol:water mixture, followed by two small portions of water. The precipitate, recrystallized from hot alcohol and dried at 105C, melts at about 152C.
B. A portion of the filtrate obtained in Identification Test A gives positive tests for Iron.
Assay: Not less than 97.0% and not more than 101.0% of C4H2FeO4, calculated on the dried basis.
Ferric Iron: Not more than 2.0%.
Lead: Not more than 2 mg/kg.
Loss on Drying: Not more than 1.5%.
Mercury: Not more than 3 mg/kg.
Sulfate: Not more than 0.2%.

Keywords: Iron Ferrous Fumarate IP BP Ph Eur EP USP Analytical Reagent FCC Food Grade CAS Number 141-01-5 Manufacturer Supplier Exporter Monograph Uses Chemical Molecular Formula Weight.

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Manufacturers

ANMOL CHEMICALS
Now maturing as Anmol Chemicals Private Limited
Representatives in Houston, Chicago and New York, USA
TEL: (OFF) +91 22 23726950, +91 22 23774610, +91 22 23723564
Taloja Navi Mumbai, INDIA

e-mail: info@anmol.org

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Last updated 26-feb-24

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Ferrous Fumarate
IP BP Ph Eur USP FCC Food Grades Manufacturers
Ferrous Fumarate