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    Also known as: 1310-45-8, Ferric subsulfate solution, Basic ferric sulfate, Iron hydroxide sulfate (fe4(oh)2(so4)5), Iron(3+);dihydroxide;pentasulfate, 3qj8ws6v8h
    Molecular Formula
    Fe4H2O22S5
    Molecular Weight
    737.7  g/mol
    InChI Key
    GDPKWKCLDUOTMP-UHFFFAOYSA-B
    FDA UNII
    3QJ8WS6V8H
    UNII-3QJ8WS6V8H
    Ferric subsulfate is a stypic or hemostatic agent that causes agglutination of surface proteins resulting in local hemostasis. It has the chemical formula Fe4(OH)2(SO4)5. It is used after superficial skin biopsies.
    1 2D Structure

    UNII-3QJ8WS6V8H

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    iron(3+);dihydroxide;pentasulfate
    2.1.2 InChI
    InChI=1S/4Fe.5H2O4S.2H2O/c;;;;5*1-5(2,3)4;;/h;;;;5*(H2,1,2,3,4);2*1H2/q4*+3;;;;;;;/p-12
    2.1.3 InChI Key
    GDPKWKCLDUOTMP-UHFFFAOYSA-B
    2.1.4 Canonical SMILES
    [OH-].[OH-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[O-]S(=O)(=O)[O-].[Fe+3].[Fe+3].[Fe+3].[Fe+3]
    2.2 Other Identifiers
    2.2.1 UNII
    3QJ8WS6V8H
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Ferric Subsulfate Solution

    2. Monsel's Solution

    2.3.2 Depositor-Supplied Synonyms

    1. 1310-45-8

    2. Ferric Subsulfate Solution

    3. Basic Ferric Sulfate

    4. Iron Hydroxide Sulfate (fe4(oh)2(so4)5)

    5. Iron(3+);dihydroxide;pentasulfate

    6. 3qj8ws6v8h

    7. Monsel's Solution

    8. Iron Dihydroxide Pentakis(sulphate)

    9. Einecs 215-179-2

    10. Unii-3qj8ws6v8h

    11. Ferric Subsulfate [usp:nf]

    12. Iron Hydroxide Sulfate

    13. Iron Subsulfate

    14. Ferric Subsulphate

    15. Ferric Subsulfate (usp)

    16. Basic Ferric Sulfate Solution

    17. Monsel's Solution [mi]

    18. Dtxsid30893846

    19. Ferric Subsulfate [vandf]

    20. Ferric Subsulphate Solution

    21. Ferric Subsulfate [who-dd]

    22. Ferric Subsulfate Decahydrate

    23. Basic Ferric Sulphate Solution

    24. Akos015910508

    25. Ferric Subsulfate [usp Impurity]

    26. Iron Dihydroxide Pentakis Sulfate

    27. Iron(iii) Dihydroxide Pentakis(sulfate)

    28. Iron Dihydroxide Pentakis Sulphate

    29. Ft-0717042

    30. D08921

    31. Iron Hydroxide Sulphate (fe4(oh)2(so4)5)

    32. Q5445335

    2.4 Create Date
    2005-08-08
    3 Chemical and Physical Properties
    Molecular Weight 737.7 g/mol
    Molecular Formula Fe4H2O22S5
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count22
    Rotatable Bond Count0
    Exact Mass737.50387 g/mol
    Monoisotopic Mass737.50387 g/mol
    Topological Polar Surface Area445 Ų
    Heavy Atom Count31
    Formal Charge0
    Complexity62.2
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count11
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Hemostatics

    Agents acting to arrest the flow of blood. Absorbable hemostatics arrest bleeding either by the formation of an artificial clot or by providing a mechanical matrix that facilitates clotting when applied directly to the bleeding surface. These agents function more at the capillary level and are not effective at stemming arterial or venous bleeding under any significant intravascular pressure. (See all compounds classified as Hemostatics.)

    4.2 FDA Pharmacological Classification
    4.2.1 Pharmacological Classes
    Parenteral Iron Replacement [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Iron [CS]

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    ABOUT THIS PAGE

    UNII-3QJ8WS6V8H Manufacturers

    A UNII-3QJ8WS6V8H manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-3QJ8WS6V8H, including repackagers and relabelers. The FDA regulates UNII-3QJ8WS6V8H manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-3QJ8WS6V8H API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

    click here to find a list of UNII-3QJ8WS6V8H manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    UNII-3QJ8WS6V8H Suppliers

    A UNII-3QJ8WS6V8H supplier is an individual or a company that provides UNII-3QJ8WS6V8H active pharmaceutical ingredient (API) or UNII-3QJ8WS6V8H finished formulations upon request. The UNII-3QJ8WS6V8H suppliers may include UNII-3QJ8WS6V8H API manufacturers, exporters, distributors and traders.

    click here to find a list of UNII-3QJ8WS6V8H suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    UNII-3QJ8WS6V8H GMP

    UNII-3QJ8WS6V8H Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

    GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

    PharmaCompass offers a list of UNII-3QJ8WS6V8H GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right UNII-3QJ8WS6V8H GMP manufacturer or UNII-3QJ8WS6V8H GMP API supplier for your needs.

    UNII-3QJ8WS6V8H CoA

    A UNII-3QJ8WS6V8H CoA (Certificate of Analysis) is a formal document that attests to UNII-3QJ8WS6V8H's compliance with UNII-3QJ8WS6V8H specifications and serves as a tool for batch-level quality control.

    UNII-3QJ8WS6V8H CoA mostly includes findings from lab analyses of a specific batch. For each UNII-3QJ8WS6V8H CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

    UNII-3QJ8WS6V8H may be tested according to a variety of international standards, such as European Pharmacopoeia (UNII-3QJ8WS6V8H EP), UNII-3QJ8WS6V8H JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNII-3QJ8WS6V8H USP).

    Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
    For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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