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Mefenamic acid structure

Mefenamic acid

  • CAS:61-68-7
  • MW:241.2851
  • MF:C15H15NO2
Mefenamic acid is a kind of nonsteroidal anti-inflammatory (NSAID) drug belonging to the anthranilic acid derivatives class. It is mainly used for the short-term treatment of mild to moderate pain from various conditions. It is also used for reducing the pain and blood loss from menstrual condition as well as prevention of migraines. Moreover, it may also be used for treating gout attacks. Its mechanism is through inhibiting both the isoforms of COX and preventing the formation of prostaglandins. It is manufactured from 2-chlorobenzoic acid and 2,3-dimethylaniline. View more+
 
1. Names and Identifiers
1.1 Name
Mefenamic acid
1.2 Synonyms
2-[(2,3-Dimethylphenyl)amino]benzoic acid; 2’,3’-dimethyl-2-diphenylaminecarboxylicaci; 2-Diphenylaminecarboxylic acid, 2',3'-dimethyl-; ac.mefenamico; Benzoic acid, 2-[(2,3-dimethylphenyl)amino]-; CI 473,CN-35355; EINECS 200-513-1; Lysalgo; Mefenacid; Mefenamate; Mefenamic Acid (200 mg); Mefenamic acid Solution, 100ppm; MefenaMic Aicd (API); MFCD00051721; N-(2,3-Dimethylphenyl)anthranilic Acid 2-(2,3-Dimethylphenylamino)benzoic Acid 2-(2,3-Xylidino)benzoic Acid; N-(2,3-Xylyl)anthranilic acid; Parkemed; Ponalar; Ponstan; Ponstel; Ponstyl; Pontal;
1.3 CAS No.
61-68-7
1.4 CID
4044
1.5 EINECS
200-513-1
1.6 Molecular Formula
C15H15NO2
1.7 Inchi
InChI=1S/C15H15NO2/c1-10-6-5-9-13(11(10)2)16-14-8-4-3-7-12(14)15(17)18/h3-9,16H,1-2H3,(H,17,18)
1.8 InChkey
HYYBABOKPJLUIN-UHFFFAOYSA-N
1.9 Canonical Smiles
CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C
1.10 Isomers Smiles
CC1=C(C(=CC=C1)NC2=CC=CC=C2C(=O)O)C
2. Properties
2.1 Appearance
light yellow solid
2.2 Storage
Refrigerator
2.3 Chemical Properties
Light Yellow Solid
2.4 Color/Form
Powder
2.5 pKa
4.2(at 25℃)
2.6 Water Solubility
insoluble
2.7 Spectral Properties
MAX ABSORPTION (0.1 N NAOH): 285 NM, 340 NM
2.8 Stability
DARKENS ON PROLONGED EXPOSURE TO LIGHT, IS STABLE @ 25 DEG, 37 DEG, & 45 DEG C.
2.9 StorageTemp
Refrigerator
3. Use and Manufacturing
3.1 Definition
ChEBI: An aminobenzoic acid that is anthranilic acid in which one of the hydrogens attached to the nitrogen is replaced by a 2,3-dimethylphenyl group. Although classed as a non-steroidal anti-inflammatory drug, its anti-inflammatory properties are considered to b minor. It is used to relieve mild to moderate pain, including headaches, dental pain, osteoarthritis and rheumatoid arthritis.
3.2 Description
Mefenamic acid (CAS 61-68-7) is a nonsteroidal anti-inflammatory drug (NSAID) that is commonly used for its analgesic and anti-inflammatory properties. It is a white crystalline powder with a chemical structure consisting of a carboxylic acid group attached to a benzene ring. Mefenamic acid is sparingly soluble in water, but it dissolves well in organic solvents such as ethanol and acetone. It has a melting point of approximately 230-235°C.

Applicable fields
Mefenamic acid is primarily used as a medication to relieve pain and inflammation. It is commonly prescribed for the treatment of menstrual pain (dysmenorrhea), rheumatoid arthritis, osteoarthritis, and other conditions that cause pain and inflammation. The mechanism of action of mefenamic acid involves inhibiting the production of prostaglandins, which are substances that contribute to pain and inflammation in the body.

Storage Conditions
Mefenamic acid should be stored in a cool and dry place, away from direct sunlight.
3.3 General Description
Mefenamic acid (Ponstel, Ponstan) is one of the oldestNSAIDs, introduced into the market in 1967 for mild tomoderate pain and for primary dysmenorrhea. It is rapidly absorbed with peak plasma levels occurring 2 to 4 hoursafter oral administration. It undergoes hepatic benzylic hydroxylationof its 3'methyl group regioselectively into twoinactive metabolites, 3'-hydroxymethylmefenamic acid andthe 3'carboxylate metabolite (via further oxidation of thebenzylic alcohol group). The parent drugs and these metabolitesare conjugated with glucuronic acid and excreted primarilyin the urine. Thus, although patients with knownliver deficiency may be given lower doses, it is contraindicatedin patients with preexisting renal dysfunction.Common side effects associated with its use include diarrhea,drowsiness, and headache. The possibility of blood disordershas also prompted limitation of its administration to 7days. It is not recommended for children or during pregnancy.
3.4 Usage
Mefenamic acid is used for the same indications as flufenamic acid. Synonyms for this drug areparkemed, ponstan, ponstel, and others.
4. Safety and Handling
4.1 Formulations/Preparations
CAPSULES: 250 MG.
4.2 Safety

Safty information about Mefenamic acid (CAS NO.61-68-7) is:
Hazard Codes:?Xn
Risk Statements: 22-40-20/21/22?
R22:Harmful if swallowed.?
R40:Limited evidence of a carcinogenic effect.?
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
Safety Statements: 22-36
S22:Do not breathe dust.?
S36:Wear suitable protective clothing.
WGK Germany: 3
RTECS: CB4550000

4.3 Specification

?Mefenamic acid , its cas register number is 61-68-7. It also can be called?Mefenamic acid [USAN:INN:BAN:JAN] ; 2-((2,3-Dimethylphenyl)amino)benzoic acid ; 2-Diphenylaminecarboxylic acid, 2',3'-dimethyl- ; Ac. mefenamico ; Ac. mefenamico [Italian] ; Acide mefenamique ; Acide mefenamique [French] ; Acide mefenamique [INN-French] ; Acido mefenamico ; Acido mefenamico [INN-Spanish] ; Acidum mefenamicum ; Acidum mefenamicum [INN-Latin] ; Anthranilic acid, N-2,3-xylyl- ; Bafhameritin-M ; Benzoic acid, 2-((2,3-dimethylphenyl)amino)- ; Benzoic acid, 2-(2,3-dimethylphenyl)amino- ; Bonabol ; Fenamin ; HL 1 ; Lysalgo ; Mefacit ; Mefedolo ; Mefenamate ; Mefenamic acid ; Mefenaminsaeure ; Mephenamic acid ; Mephenaminic acid ; Methenamic acid ; Mycasaal ; N-(2,3-Dimethylphenyl)anthranilic acid ; N-(2,3-Xylyl)-2-aminobenzoic acid ; N-2,3-Xylylanthranilic acid ; Namphen ; Parkemed ; Ponalar ; Ponstan ; Ponstan forte ; Ponstel ; Rolan ; Tamany Bonsan ; Tanston ; Vialidon . It is a?light yellow solid. Since?it plays a significant role in mefenamic acid elimination, patients with known liver deficiency may be prescribed lower doses. Kidney deficiency may also cause accumulation of the drug and its metabolites in the excretory system. Therefore patients suffering from renal conditions should not be prescribed mefenamic acid.

4.4 Toxicity

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
cat LD50 intravenous 100mg/kg (100mg/kg) ? Current Medical Research and Opinion. Vol. 4, Pg. 17, 1976.
man TDLo oral 14285ug/kg/3D (14.285mg/kg) ? British Journal of Clinical Practice. Vol. 49, Pg. 161, 1995.
man TDLo oral 14285ug/kg/3D (14.285mg/kg) ? British Journal of Clinical Practice. Vol. 49, Pg. 161, 1995.
man TDLo oral 257mg/kg/12D- (257mg/kg) KIDNEY, URETER, AND BLADDER: "CHANGES IN TUBULES (INCLUDING ACUTE RENAL FAILURE, ACUTE TUBULAR NECROSIS)" British Medical Journal. Vol. 291, Pg. 661, 1985.
man TDLo oral 840mg/kg/6W-I (840mg/kg) GASTROINTESTINAL: ULCERATION OR BLEEDING FROM LARGE INTESTINE

GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"
British Medical Journal. Vol. 287, Pg. 1626, 1983.
mouse LD50 intramuscular 400mg/kg (400mg/kg) ? Pharmaceutical Chemistry Journal Vol. 17, Pg. 353, 1983.
mouse LD50 intraperitoneal 120mg/kg (120mg/kg) ? Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 36, 1969.
mouse LD50 intravenous 96mg/kg (96mg/kg) ? Yakugaku Zasshi. Journal of Pharmacy. Vol. 89, Pg. 1392, 1969.
mouse LD50 oral 525mg/kg (525mg/kg) ? Journal de Pharmacologie. Vol. 2, Pg. 259, 1971.
mouse LDLo subcutaneous > 2gm/kg (2000mg/kg) PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE)

BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Arzneimittel-Forschung. Drug Research. Vol. 20, Pg. 1579, 1970.
rat LD50 intraperitoneal 327mg/kg (327mg/kg) ? Toxicology and Applied Pharmacology. Vol. 18, Pg. 185, 1971.
rat LD50 intravenous 112mg/kg (112mg/kg) ? Current Medical Research and Opinion. Vol. 4, Pg. 17, 1976.
rat LD50 oral 740mg/kg (740mg/kg) BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)

BEHAVIORAL: ATAXIA

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION
Toho Igakkai Zasshi. Journal of Medical Society of Toho University. Vol. 28, Pg. 99, 1981.
women LDLo oral 280mg/kg/2W-I (280mg/kg) LIVER: LIVER FUNCTION TESTS IMPAIRED

KIDNEY, URETER, AND BLADDER: "CHANGES IN TUBULES (INCLUDING ACUTE RENAL FAILURE, ACUTE TUBULAR NECROSIS)"

BLOOD: OTHER HEMOLYSIS WITH OR WITHOUT ANEMIA
Drug Safety. Vol. 6, Pg. 230, 1991.
women TDLo oral 20mg/kg/4D-I (20mg/kg) GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF ENDOCRINE PANCREAS Canadian Medical Association Journal. Vol. 126, Pg. 894, 1982.
women TDLo oral 450mg/kg (450mg/kg) SENSE ORGANS AND SPECIAL SENSES: MYDRIASIS (PUPILLARY DILATION): EYE

BEHAVIORAL: TOXIC PSYCHOSIS

BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
South African Medical Journal. Vol. 67, Pg. 823, 1985.
women TDLo unreported 120mg/kg/4D (120mg/kg) BEHAVIORAL: WITHDRAWAL

SKIN AND APPENDAGES (SKIN): "DERMATITIS, OTHER: AFTER SYSTEMIC EXPOSURE"
Lancet. Vol. 2, Pg. 745, 1980.

5. MSDS

2.Hazard identification

2.1 Classification of the substance or mixture

Acute toxicity - Oral, Category 4

2.2 GHS label elements, including precautionary statements

Pictogram(s)
Signal word

Warning

Hazard statement(s)

H302 Harmful if swallowed

Precautionary statement(s)
Prevention

P264 Wash ... thoroughly after handling.

P270 Do not eat, drink or smoke when using this product.

Response

P301+P312 IF SWALLOWED: Call a POISON CENTER/doctor/\u2026if you feel unwell.

P330 Rinse mouth.

Storage

none

Disposal

P501 Dispose of contents/container to ...

2.3 Other hazards which do not result in classification

none

6. NMR Spectrum
13C NMR : Predict  
1H NMR : Predict  
Predict 1H proton NMR  
Mass spectrum (electron ionization)  
7. Synthesis Route
61-68-7Total: 15 Synthesis Route
 
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8. Precursor and Product
precursor:
product:
9. Computed Properties
10.Other Information
Usage
Mefenamic acid has demonstrated antiproliferative activity against colorectal cancer cells. It has Analgesic, Anti-inflammatory activity. It is used to relieve mild to moderate pain, including headaches, dental pain, osteoarthritis and rheumatoid arthritis.
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12. Related Questions
What are the applications and effects of Mefenamic Acid in pharmaceuticals?Mefenamic Acid is a commonly used drug ingredient with multiple applications and benefits. This article will explore the applications and effects of Mefenamic Acid in the pharmaceutical industry. Effe..
Does Mefenamic Acid Cause Liver Damage?Mefenamic acid, also known as MFA, is a nonsteroidal anti-inflammatory drug (NSAID) primarily used for the treatment of acute pain. It has been associated with rare cases of acute liver injury in clin..
What is Mefenamic Acid and How Can It Help You?Mefenamic acid is a medication used for its anti-inflammatory and analgesic properties. It is effective in treating conditions such as headaches, toothaches, rheumatoid arthritis, and menstrual pain, ..
What is Mefenamic Acid and its Uses?Mefenamic acid, also known as Mefenamic acid and Ponstel, is a nonsteroidal anti-inflammatory drug (NSAID) used for the treatment of various types of pain, including menstrual pain. It is marketed as ..
13. Realated Product Infomation
 
 
 
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