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Merck
CN

JN0004

Tolmetin sodium dihydrate

≥98% (HPLC)

Synonym(s):

Tolmetin sodium salt dihydrate, 1-Methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic acid sodium salt dihydrate, Sodium 2-(1-methyl-5-(4-methylbenzoyl)-1H-pyrrol-2-yl)acetate dihydrate, 1-Methyl-5-(p-toluoyl)pyrrole-2-acetic acid sodium salt dihydrate

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About This Item

Linear Formula:
C15H14NO3Na · 2H2O
CAS Number:
64490-92-2
Molecular Weight:
315.30
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
MFCD00150761

Key Documents

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InChI

1S/C15H15NO3.Na.2H2O/c1-10-3-5-11(6-4-10)15(19)13-8-7-12(16(13)2)9-14(17)18;;;/h3-8H,9H2,1-2H3,(H,17,18);;2*1H2/q;+1;;/p-1

SMILES string

[Na+].[H]O[H].[H]O[H].Cc1ccc(cc1)C(=O)c2ccc(CC([O-])=O)n2C

InChI key

QQILXENAYPUNEA-UHFFFAOYSA-M

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

H2O: 2 mg/mL, clear

storage temp.

room temp

Gene Information

human ... PTGS1(5742), PTGS2(5743)

Biochem/physiol Actions

Tolmetin sodium is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits prostaglandin synthetase in vitro and reduces plasma levels of prostaglandin E. Tolmetin sodium exhibits anti-inflammatory, analgesic and antipyretic activity Its precise mechanism of is unknown. Tolmetin is used to treat rheumatoid arthritis, osteoarthrosis, pain, and ankylosing spondylitis.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000311717
0000311717
0000078363
0000078361
0000073467

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J Davies et al.
Current medical research and opinion, 7(2), 115-120 (1980-01-01)
A double-blind crossover study was carried out in 21 patients with osteoarthrosis of the hip to compare the effectiveness and tolerance of 1200 mg tolmetin sodium daily with 75 mg indomethacin daily. Each drug was given in 3 equally divided
F J Persico et al.
The Journal of pharmacology and experimental therapeutics, 247(3), 889-896 (1988-12-01)
The glycine amide of tolmetin sodium (TGA) functions as a prodrug and was demonstrated to be more potent than the parent compound as an inhibitor of developing and established adjuvant arthritis in the female Lewis rat. In contrast, the glycine
Afaf A Ramadan et al.
Journal of pharmaceutical investigation, 48(6), 673-683 (2019-01-01)
The objective of the present study was to develop rectal mucoadhesive hydrogels loaded with Tolmetin Sodium, a non-steroidal anti-inflammatory drug, for prolonged duration of action and increased bioavailability. Fourteen formulae were prepared with different types and concentrations of polymers as

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