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CAS RN: 61-68-7 | Product Number: M1782

Mefenamic Acid


Purity: >98.0%(T)
Synonyms:
  • N-(2,3-Dimethylphenyl)anthranilic Acid
  • 2-(2,3-Dimethylphenylamino)benzoic Acid
  • 2-(2,3-Xylidino)benzoic Acid
Product Documents:
25G
€29.00
15   ≥40 
100G
€79.00
2   4  
500G
€252.00
1   11  

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*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Product Number M1782
Purity / Analysis Method >98.0%(T)
Molecular Formula / Molecular Weight C__1__5H__1__5NO__2 = 241.29 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 61-68-7
Reaxys Registry Number 2216243
PubChem Substance ID 87558870
SDBS (AIST Spectral DB) 51771
Merck Index (14) 5798
MDL Number

MFCD00051721

Specifications
Appearance White to Light yellow powder to crystal
Purity(Neutralization titration) min. 98.0 %
NMR confirm to structure
Properties (reference)
Melting Point 230 °C
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H302 : Harmful if swallowed.
H361 : Suspected of damaging fertility or the unborn child.
H362 : May cause harm to breast-fed children.
H371 : May cause damage to organs.
H370 : Causes damage to organs.
H372 : Causes damage to organs through prolonged or repeated exposure.
Precautionary Statements P263 : Avoid contact during pregnancy and while nursing.
P260 : Do not breathe dust.
P202 : Do not handle until all safety precautions have been read and understood.
P201 : Obtain special instructions before use.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P308 + P311 : IF exposed or concerned: Call a POISON CENTER/doctor.
Related Laws:
EC Number 200-513-1
RTECS# CB4550000
Transport Information:
HS Number 2922498590
Application
Mefenamic Acid: A Non-Selective Non-Steroidal Anti-Inflammatory Drug (NSAID)

Mefenamic acid is a non-steroidal anti-inflammatory drug (NSAID) with strong analgesic activity. It is a non-selective cyclooxygenase (COX) inhibitor. COX directs the formation of several key mediators of inflammation called prostaglandins. Thus, mefenamic acid reduces the synthesis of prostaglandins. Mefenamic acid is metabolized principally by CYP2C9. Recently, some unique biological properties of mefenamic acid have also been reported. (The product is for research purpose only.)

References


PubMed Literature


TCIMAIL
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Other Documents

Life Science
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