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Nafamostat Mesylate

CAS 82956-11-4C21H25N5O8S2MW 539.6

Nafamostat Mesylate (CAS 82956-11-4) — formula C21H25N5O8S2, molecular weight 539.6; category organic chemicals.

Product Overview

CAS Number82956-11-4
Molecular FormulaC21H25N5O8S2
Molecular Weight539.6
CategoryOrganic Chemicals

Technical Profile

What this product is

Nafamostat Mesylate is a carbon-based organic compound with CAS registry number 82956-11-4 and molecular formula C21H25N5O8S2 (molecular weight 539.6), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 82956-11-4

Its molecular formula C21H25N5O8S2 comprises 21 C, 25 H, 5 N, 8 O, 2 S atoms.

Also known as: Nafamostat Mesylate

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Nafamostat Mesylate?

The CAS registry number of Nafamostat Mesylate is 82956-11-4.

What is the molecular formula and molecular weight of Nafamostat Mesylate?

Molecular formula C21H25N5O8S2, molecular weight 539.6.

What other names is Nafamostat Mesylate known by?

It is also registered under: Nafamostat Mesylate.

Which category does Nafamostat Mesylate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Nafamostat Mesylate (CAS 82956-11-4), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number82956-11-4
PubChem CID5311180
Molecular formulaC21H25N5O8S2
IUPAC name(6-carbamimidoylnaphthalen-2-yl) 4-(diaminomethylideneamino)benzoate;methanesulfonic acid
UNII (FDA)1D2T74921W

Computed descriptors

Molecular Weight539.6
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count10
Rotatable Bond Count5
Exact Mass539.11445512
Monoisotopic Mass539.11445512
Topological Polar Surface Area266
Heavy Atom Count36

Documented uses on record

    Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.Agents that prevent BLOOD CLOTTING.

    Synonyms and trade names

    Nafamostat mesylate; 82956-11-4; nafamostat mesilate; FUT-175; Nafamstat Mesilate; Ronastat; Nafamostat dimethanesulfonate; 1D2T74921W; Benzoic acid, 4-[(aminoiminomethyl)amino]-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate; DTXSID7046128; FUT 175; 6-Amidino-2-naphthyl 4-guanidinobenzoate dimethanesulfonate; CKD-314; Benzoic acid, 4-((aminoiminomethyl)amino)-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate; RefChem:164397; FUT175

    GHS hazard classification

    Reported hazard statementsH361 (95.3%)

    H361 (95.3%): Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]

    P203, P280, P318, P405, and P501 (click each P-code to see the statement)

    What the public record says

    Nafamostat Mesylate · CAS 82956-11-4 · C21H25N5O8S2. UNII 1D2T74921W.

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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