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Loxoprofen Sodium Hydrate

CAS 226721-96-6C15H21NaO5MW 304.31

Loxoprofen Sodium Hydrate (CAS 226721-96-6) — formula C15H21NaO5, molecular weight 304.31; category organic chemicals.

Product Overview

CAS Number226721-96-6
Molecular FormulaC15H21NaO5
Molecular Weight304.31
CategoryOrganic Chemicals

Technical Profile

What this product is

Loxoprofen Sodium Hydrate is a carbon-based organic compound with CAS registry number 226721-96-6 and molecular formula C15H21NaO5 (molecular weight 304.31), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 226721-96-6

Its molecular formula C15H21NaO5 comprises 15 C, 21 H, 1 Na, 5 O atoms.

Also known as: Loxoprofen Sodium Hydrate · 洛索洛芬钠水合物

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Loxoprofen Sodium Hydrate?

The CAS registry number of Loxoprofen Sodium Hydrate is 226721-96-6.

What is the molecular formula and molecular weight of Loxoprofen Sodium Hydrate?

Molecular formula C15H21NaO5, molecular weight 304.31.

What other names is Loxoprofen Sodium Hydrate known by?

It is also registered under: Loxoprofen Sodium Hydrate, 洛索洛芬钠水合物.

Which category does Loxoprofen Sodium Hydrate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for Loxoprofen Sodium Hydrate (CAS 226721-96-6), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number226721-96-6
PubChem CID23674745
Molecular formulaC15H21NaO5
IUPAC namesodium;2-[4-[(2-oxocyclopentyl)methyl]phenyl]propanoate;dihydrate
UNII (FDA)Z2DR42L11Y

Computed descriptors

Molecular Weight304.31
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass304.12866805
Monoisotopic Mass304.12866805
Topological Polar Surface Area59.2
Heavy Atom Count21

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.

Synonyms and trade names

Sodium 2-(4-(2-oxocyclopentylmethyl)phenyl)propionate dihydrate; RefChem:154144; Loxoprofen sodium dihydrate; 226721-96-6; Loxoprofen Sodium Salt Dihydrate; Oxeno; Lobu; Loxoprofen sodium hydrate; Loxoprofen sodium [Mart.]; Loxoprofen sodium hydrate [jp]; sodium;2-[4-[(2-oxocyclopentyl)methyl]phenyl]propanoate;dihydrate; Loxoprofen (monosodium); MFCD01745788; Lobu; Loxonin;CS 600; Z2DR42L11Y; Monosodium 2-(4-((2-oxocyclopentyl)methyl)phenyl)propanoate dihydrate

GHS hazard classification

Reported hazard statementsH301 (100%)

H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

P264, P270, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)

What the public record says

Loxoprofen Sodium Hydrate · CAS 226721-96-6 · C15H21NaO5. UNII Z2DR42L11Y.

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

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Supplier: Jinan Shenghe Chemical Co., Ltd.

中文页面: 洛索洛芬钠水合物

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