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About This Item
Empirical Formula (Hill Notation):
C13H16N3O4S · Na · H2O
CAS Number:
Molecular Weight:
351.35
UNSPSC Code:
12352200
NACRES:
NA.77
Product Name
Metamizole sodium hydrate, ≥98% (HPLC)
SMILES string
[Na+].[S](=O)(=O)([O-])CN(C)c1[c]([n]([n](c1C)C)c2ccccc2)=O.O
InChI
1S/C13H17N3O4S.Na.H2O/c1-10-12(14(2)9-21(18,19)20)13(17)16(15(10)3)11-7-5-4-6-8-11;;/h4-8H,9H2,1-3H3,(H,18,19,20);;1H2/q;+1;/p-1
InChI key
UNZIDPIPYUMVPA-UHFFFAOYSA-M
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
H2O: 25 mg/mL, clear
storage temp.
2-8°C
Quality Level
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Related Categories
Biochem/physiol Actions
Metamizole (Dipyrone) is a potent analgesic and antipyretic.
Metamizole (Dipyrone) is a potent analgesic and antipyretic. Metamizole inhibits prostaglandin synthesis in both the periphery and the central nervous system. Metamizole may act as a prodrug. It is rapidly hydrolyzed to N-methyl-4-aminoantipyrine (MAA) and 4-aminoantipyrine (AA) which inhibit cyclo-oxygenase activity and can be further acylated with arachidonic acid forming compounds that bind to central and peripheral cannabinoid (CB1 and CB2) receptors and TRPV1 receptors. It is believed that these metabolites play a major role in metamizole activity. Metamizole has been withdrawn from clinical use in several countries because of a side-effect of agranulocytosis in some patients.
General description
Metamizole sodium is a nonsteroidal anti-inflammatory drug (NSAID). It is widely used as an analgesic and antipyretic agent.
signalword
Warning
hcodes
Hazard Classifications
Repr. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
涉药品监管产品
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Acute kidney injury associated with metamizole sodium ingestion.
Hassan K, et al.
Renal Failure, 33(5), 544-547 (2011)
Diéssica Padilha Dalenogare et al.
Pharmaceuticals (Basel, Switzerland), 14(8) (2021-08-29)
Headaches are frequently described in progressive multiple sclerosis (PMS) patients, but their mechanism remains unknown. Transient receptor potential ankyrin 1 (TRPA1) was involved in neuropathic nociception in a model of PMS induced by experimental autoimmune encephalomyelitis (PMS-EAE), and TRPA1 activation
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