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Specifications, Properties, Uses, SDS of Iron Fumarate or Ferrous Fumarate USP BP Ph Eur IP FCC Food Grade Manufacturer Supplier Exporter Wholesale & Small Packs, CAS Number 141-01-5.
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We supply fine and speciality chemicals, pharmaceutical excipients, mineral fortifiers in chemically pure, analytical reagent grade, IP BP USP Ph Eur EP JP and other pharmaceutical grade monograph including FCC Food grade chemicals and Nutraceuticals at best prices. We and/or our associated units have all the facilities to supply as per cGMP standard observing good manufacturing practice and good laboratory practice. We can assure low microbial count and also offer a test certificate for the same. We maintain warehouses across USA, India, and UAE. Our group exports to USA, Canada, Mexico, Argentina, Brazil, Chile, Korea, Malaysia, Thailand, Indonesia, Europe, and several other parts of the world. We supply in wholesale container loads to small pack of few grams. Solid products may be specified for it size and shape as desired by the buyer.
Iron Fumarate or Ferrous Fumarate CAS Number 141-01-5For Properties Specifications Uses of Iron Fumarate or Ferrous Fumarate Click Properties, Specifications, Uses, Price, Process of Iron Fumarate or Ferrous Fumarate Manufacturer.
For For SDS MSDS Sheet of Iron Fumarate or Ferrous Fumarate Click SDS Safety Data Sheet MSDS Sheet of Iron Fumarate or Ferrous Fumarate Manufacturer.
The Properties, Specifications, Monograph and Uses of Iron Fumarate or Ferrous Fumarate:
Iron(II) fumarate or Ferrous fumarate, is the iron(II) salt of fumaric acid, occurring as a reddish-orange powder, used to supplement iron intake. It has the chemical formula C4H2FeO4. It is generally used in iron supplements and in pharmaceutical industries.
Specifications of Ferrous Fumarate FCC Food Grade
Iron (II) Fumarate FCC
C4H2FeO4 --- Formula weight 169.90 --- CAS: 141-01-5DESCRIPTION
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 105, 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%.
Ferrous Fumarate BP Grade Ph Eur
C4H2FeO4 --- 169.9 --- 141-01-5DEFINITION
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
C4H2FeO4 --- 169.90
2-Butenedioic acid, (E)-, iron(2+) salt.
Iron(2+) fumarate [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.
Ferrous Fumarate IP Grade
We also manufacture Micro-Encapsulated Ferrous Fumarate, having core of Ferrous Fumarate and coating of vegetable oil or mono and diglycerides or as desired by the buyer. Such encapsulation makes the product slow release or extended release.
Please visit Ferrous Fumarate or Micro-encapsulated Ferrous Fumarate.
The MSDS-SDS Hazard Statement of Iron Fumarate or Ferrous Fumarate:
Iron Fumarate or Ferrous Fumarate SDS, Safety Data Sheet
MSDS Sheet, Material Safety Data Sheet 29-Jun-21Section 1: Chemical Product and Identification
Product Name & Other Names: Ferrous fumarate or Iron fumarate or Fumaric acid ferrous salt.
CAS#: 141-01-5
EINECS EC-No.: 205-447-7
Chemical Formula: C4H2FeO4
Molecular Weight: 169.9
Relevant uses and uses advised against (if any): Laboratory and Industrial Manufacturing.
SUPPLIER: As per letterhead.Section 2: Hazards Identification
GHS, Globally Harmonized System Classification in accordance with 29 CFR 1910
Classification according to Regulation (EC) No 1272/2008Not 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.Labeling according to GHS & Regulation (EC) No 1272/2008
GHS Label Elements
NONESignal Word: None
Precautionary statements:
P261: Avoid breathing dust/fume/gas/mist/vapors/spray.
P302+P352 - IF ON SKIN: Wash with plenty of soap and water.
P303+P361+P353 - IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower.
P304 + P340 - IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P337+313: If eye irritation persists get medical advice/attention.Section 3: Composition and Information on Ingredients
Product Name & Other Names: Ferrous fumarate or Iron fumarate or Fumaric acid ferrous salt.
CAS#: 141-01-5
EINECS EC-No.: 205-447-7Section 4: First Aid Measures
Always seek medical attention after first aid measures are provided.
Eye Contact: In case of contact, immediately flush eyes with plenty of water for at least 15 minutes. Get medical attention.
Skin Contact: In case of contact, immediately flush skin with plenty of water. Cover the irritated skin with an emollient. Thoroughly clean shoes and clothes before reuse. Get medical attention.
Inhalation: If Ferrous Fumarate is inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical attention.
Ingestion: Do NOT induce vomiting unless directed to do so by medical personnel. Never give anything by mouth to an unconscious person. If large quantities of this material are swallowed, call a physician immediately.Section 5: Fire and Explosion Data
Flammability of the Product: Ferrous Fumarate may be combustible at high temperature.
Auto-Ignition Temperature: Not available.
Products of Combustion: Some metallic oxides CO, CO2 and fumes.
Fire Hazards in Presence of Various Substances: Slightly flammable in presence of heat. Non-flammable in presence of shocks.
Explosion Hazards in Presence of Various Substances: Slightly explosive in presence of open flames and sparks. Non-explosive in presence of shocks.
Fire Fighting Media and Instructions:
Small Fire: Use DRY chemical powder.
Large Fire: Use water spray, fog, or foam. Avoid water jet.
Extinguishing Media Not recommended: Avoid using solid water jet as it may scatter the fire.
Special Information: In the event of a fire, wear full protective clothing and NIOSH-approved self-contained breathing apparatus with full face piece operated in the pressure demand or other positive pressure mode. At high temperatures under fire conditions, it may produce toxic or irritating fumes. Fire-extinguishing work is done from the windward and the suitable fire-extinguishing method according to the surrounding situation is used. Uninvolved persons should evacuate to a safe place.Section 6: Accidental Release Measures
Personal precautions, protective equipment, and emergency procedures: Ventilate area of leak or spill. Avoid breathing dust/fumes/gas/mist/vapors/spray. Use individual protective equipment (waterproof boots, suitable protective clothing, safety glasses, etc.). Restrict unprotected personnel from the area. Prevent any contact with hot surfaces. Do not approach facing the wind. Do not touch the spilled material.
Environmental precautions: Do not let the product enter drains, soil, or water sources.
Methods and materials used for containment cleanup procedures and Storage: Contain spilled material. Cover with an inert, non-combustible absorbent material, (e.g. sand, earth, diatomaceous earth, vermiculite). Vacuum or sweep-up and remove to an approved disposal container. Finish cleaning by spreading water on the contaminated surface and allow to evacuate as per law.Section 7: Handling and Storage
Precautions for safe handling: Apply according to good manufacturing and industrial hygiene practices. Ensure proper ventilation. In case of insufficient ventilation, wear suitable respiratory equipment. Wash thoroughly after handling. Do not drink, eat, or smoke while handling. Avoid contact with skin, eyes, and clothing. Minimize dust generation. Avoid breathing dust/fumes/gas/mist/vapors/spray. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation. Use individual protective equipment (waterproof boots, suitable protective clothing, safety glasses, etc.). Prevent any contact with hot surfaces.
Conditions for safe storage, including any incompatibilities: Store in cool, dry, and ventilated area away from heat sources and protected from sunlight in tightly closed original container. Keep air contact to a minimum. Store protected from heat, sparks and ignition sources and incompatible materials. Avoid contact with skin and eyes. Avoid inhalation of dust/mist/vapor. Do not store with incompatible materials like strong oxidizing agents.Section 8: Exposure Controls/Personal Protection
Exposure Limits: TWA 1 mg/m3 - US. ACGIH Threshold Limit Values (2011).
Engineering Controls: Use process enclosures, local exhaust ventilation, or other engineering controls to keep airborne levels below recommended exposure limits. If user operations generate dust, fume, or mist, use ventilation to keep exposure to airborne contaminants below the exposure limit.
Ventilation System: A system of local and/or general exhaust is recommended to keep employee exposures as low as possible. Local exhaust ventilation is generally preferred because it can control the emissions of the contaminant at its source, preventing dispersion of it into the general work area.
Personal Respirators (NIOSH Approved): For conditions of use where exposure to dust or mist is apparent and engineering controls are not feasible, a particulate respirator may be worn. For emergencies or instances where the exposure levels are not known, use a full-face positive-pressure, air-supplied respirator.
Skin Protection: Wear protective gloves and clean body-covering clothing.
Eye Protection: Use chemical safety goggles and/or full face shield where dusting or splashing of solutions is possible. Maintain eye wash fountain and quick-drench facilities in work area.
Other Control Measures: Maintain good housekeeping in work area. Dust deposits on floors and other surfaces may pick up moisture and cause the surfaces to become slippery and present safety hazards. Handle in accordance with good industrial hygiene and safety practice. Wash hands after handling.Section 9: Physical and Chemical Properties
Appearance: Crystalline or powdered solid.
Odor: Odorless.
Odor threshold: Not available.
pH: Not available.
Relative density: around 2.4
Melting Point: 280C
Initial boiling point and boiling range: Not available.
Flash point: Not available.
Auto-ignition temperature: Not available.
Decomposition temperature: Not available.
Upper/lower flammability or explosive limits: Not available.
Vapor pressure: Not available.
Vapor density: Not available.
Evaporation rate: Not available.
Flammability (solid, gas): Not available.
Partition coefficient: n-octanol/water: Not available.
Solubility: Soluble in water.
Viscosity: Not available.
Chemical Formula: C4H2FeO4
Molecular Weight: 169.9Section 10: Stability and Reactivity Data
Stability: It is stable.
Conditions of Instability: Excessive heat, dust generation
Incompatibility with various substances: Strong oxidizing agents.
Polymerization: Will not occur.Section 11: Toxicological Information
Toxicity to Animals:
LD50/oral/rat = 3850 mg/kg.
LD50/oral/mouse = 1570 mg/kg.
Carcinogenicity: No component of this product present at levels greater than or equal to 0.1% is identified as probable or confirmed human carcinogen by IARC, ACGIH, OSHA and NTP.
Mutagenic Effects: Not available.
Teratogenic Effects: Not available.
Environmental Toxicity: Not available.Section 12: Ecological Information
Toxicity to fish: Not available.
Products of Biodegradation: Possibly hazardous short-term degradation products are not likely. However, long term degradation products may arise.
Results of PBT and vPvB assessment: This substance/mixture contains no components considered to be either persistent, bioaccumulative and toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.Section 13: Disposal Considerations
Waste Disposal: Waste must be disposed of in accordance legal regulations.
Section 14: Transport Information
Land Transport DOT USA & ADR/RID Europe: Not dangerous goods.
Sea Transport TDG/IMDG: Not dangerous goods.
Air Transport IATA/ICAO: Not dangerous goods.Section 15: Other Regulatory Information
USA:
DISCLAIMER: The information and recommendations set forth herein (hereinafter "Information") are presented in good faith and believed correct as of the date hereof. It is compiled from various sources, and it is not necessarily all inclusive nor fully adequate in every circumstance. In addition, these suggestions should not be confused with nor followed in violation of applicable laws, regulations, rules, or insurance requirements applicable. This SDS MSDS sheet is intended only as a guide to the appropriate precautionary handling of the material by a professionally trained person using this product. Individuals receiving the information must exercise their independent judgment in determining its appropriateness for a particular purpose. This shall not constitute a guarantee for any specific product features and shall not establish a legally valid contractual relationship. In no case shall our company be liable to loss or damages by the product user.
California Proposition 65 Chemicals known to cause cancer: Substance is not listed.
Section 16 - Additional Information
Iron Fumarate or Ferrous Fumarate Manufacturers, Suppliers, Exporters, Wholesalers:
King of Chemicals manufacturers
Plot No. 2900/46&47 + 2900/163to167, GIDC, Ankleshwar, Dist. Bharuch, India
India, USA, UAE
TEL: (Office) 91-22-23774610, 91-22-23723564email: info@kingofchemicals.com
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If I give you “My Word” Nobody can undo it.
If I sign an “Agreement” my Lawyer will undo itOur products are for industrial and laboratory use only. The user must test the material before use. We are not dispensing chemists or druggist and do not offer over the counter type (OTC) products for medical use by individuals.
We and our associates manufacture pure chemicals surpassing Monograph Specifications of Analytical Reagent Standards, British & European Pharmacopoeia BP Ph Eur EP Standard, US Pharmacopoeia USP NF Standard, Indian Pharmacopoeia IP Standard, Japan Pharmacopoeia JP Standard, FCC Food Grade Standard.Micro-encapsulated Ferrous Fumarate
Micro-encapsulated Ferric Pyrophosphate
Micro-encapsulated Ferrous Sulfate
Ferrous Bisglycinate or Iron Glycinate