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Carprofen

Carprofen Structure
CAS No.
53716-49-7
Chemical Name:
Carprofen
Synonyms
c5720;imadyl;rimadyl;Ridamyl;Caroline;CARPROFEN;kanujofen;carprofeno;rac Carprofen;Carprofen CRS
CBNumber:
CB0663159
Molecular Formula:
C15H12ClNO2
Molecular Weight:
273.71
MOL File:
53716-49-7.mol
Modify Date:
2024/5/31 17:33:32

Carprofen Properties

Melting point 186-1880C
Boiling point 509.1±35.0 °C(Predicted)
Density 1.2011 (rough estimate)
refractive index 1.5200 (estimate)
storage temp. Sealed in dry,2-8°C
solubility DMSO: soluble20mg/mL, clear
form powder
pka 4.84±0.30(Predicted)
color white to beige
Merck 14,1862
InChI InChI=1S/C15H12ClNO2/c1-8(15(18)19)9-2-4-11-12-7-10(16)3-5-13(12)17-14(11)6-9/h2-8,17H,1H3,(H,18,19)
InChIKey PUXBGTOOZJQSKH-UHFFFAOYSA-N
SMILES N1C2=C(C=C(Cl)C=C2)C2=C1C=C(C(C)C(O)=O)C=C2
CAS DataBase Reference 53716-49-7(CAS DataBase Reference)
EPA Substance Registry System 9H-Carbazole-2-acetic acid, 6-chloro-.alpha.-methyl- (53716-49-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P301+P330+P331+P310
Hazard Codes  T,Xn
Risk Statements  25-36/37/38-20/21/22
Safety Statements  45-36-26
RIDADR  UN 2811
WGK Germany  3
RTECS  FE3180000
HazardClass  6.1
PackingGroup  III
HS Code  29339900
Toxicity LD50 orally in mice: 400 mg/kg (Berger, Corraz)
NFPA 704
0
2 0

Carprofen price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML1713 Carprofen ≥97% (HPLC) 53716-49-7 10MG ₹8302.78 2022-06-14 Buy
Sigma-Aldrich(India) SML1713 Carprofen ≥97% (HPLC) 53716-49-7 50MG ₹33438.43 2022-06-14 Buy
Sigma-Aldrich(India) PHR1452 Carprofen Pharmaceutical Secondary Standard; Certified Reference Material 53716-49-7 1G ₹10857.48 2022-06-14 Buy
Sigma-Aldrich(India) 33975 Carprofen VETRANAL?, analytical standard 53716-49-7 100MG ₹11355.43 2022-06-14 Buy
TCI Chemicals (India) C2701 Carprofen 53716-49-7 1G ₹10300 2022-05-26 Buy
Product number Packaging Price Buy
SML1713 10MG ₹8302.78 Buy
SML1713 50MG ₹33438.43 Buy
PHR1452 1G ₹10857.48 Buy
33975 100MG ₹11355.43 Buy
C2701 1G ₹10300 Buy

Carprofen Chemical Properties,Uses,Production

Description

Carprofen is a non-steroidal anti-inflammatory drug (NSAID) commonly used in animals to combat pain and inflammation, particularly as associated with osteoarthritis. Like many NSAIDs, carprofen inhibits both cyclooxygenases COX-1 and COX-2 (IC50s = 22.3 and 3.9 μM, respectively). It also inhibits fatty acid amide hydrolase (IC50 = 74 μM), blocking the metabolism of the cannabinoid receptor ligand, arachidonoyl ethanolamide .

Chemical Properties

Off-White Crystalline Solid

History

Carprofen has strong anti-inflammatory and analgesic activity. It has been used in human medicine for more than 10 years at doses of 150 to 600 mg per day. In human clinical trials, Carprofen was generally well tolerated. Most adverse reactions were transient and mild, such as gastrointestinal discomfort or pain and nausea. The incidence of side effects in humans is similar to that of aspirin and other NSAIDs. However, for commercial reasons, carprofen has been withdrawn from the market and is no longer available for human use.

Uses

Carprofen is a non steroidal anti-inflammatory that is used by veterinarians for the relief of arthritic systems in dogs. It can be used for joint pain or post operative inflammation. Carprofen, is al so used for the relief from pain and inflammation associated with osteoarthritis, hip dysplasia and other joint issues.

Definition

ChEBI: Propanoic acid in which one of the methylene hydrogens is substituted by a 6-chloro-9H-carbazol-2-yl group. A non-steroidal anti-inflammatory drug, it is no longer used in human medicine but is still used for treatment of arthritis in elderly dogs.

Mechanism of action

Carprofeng is a non-narcotic NSAID with analgesic and antipyretic properties. It acts in the same way as most NSAIDs in that Carprofeng acts by inhibiting cyclooxygenase (COX), which selectively inhibits COX-2, thereby inhibiting the release of several prostaglandins involved in the chronic inflammatory response that is thought to be present in canine OA.

Side effects

Common side effects of Carprofeng in dogs include vomiting, diarrhoea, loss of appetite, constipation, behavioural changes; and in severe cases, black stools, gastrointestinal ulcers and gastrointestinal haemorrhage, jaundice, skin changes, involuntary muscle movements, and kidney damage (increased thirst, increased urination, and refusal to eat).

Global( 417)Suppliers
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Carprofen Spectrum

6-CHLORO-ALPHA-METHYL-9H-CARBAZOLE-2-ACETIC ACID (+/-)-6-chloro-alpha-methylcarbazole-2-acetic acid CARPROFEN 2-(6-chloro-9H-carbazol-2-yl)propanoic acid methylcarbazole-2-acetic acid Carprofen,6-Chloro-α-methyl-9H-carbazole-2-acetic acid Carprofen (200 mg) Carprofen (200 mg) (AS) rac Carprofen (dl)-6-Chloro-α-Methylcarbazole- 2-acetic Acid 9H-Carbazole-2-acetic acid, 6-chloro-α-methyl- Carprofen Solution, 100ppm Carprofen, >=98% 33975 - VETRANAL, analytical standard Ro-20-5720/000 6-Chloro-a-methyl-9H-carbazole-2-acetic Acid 6-Chloro-α-methylcarbazole-2-acetic acid 9H-Carbazole-2-acetic acid, 6-chloro-.alpha.-methyl- 6-chloro-α-methyl-9h-carbazole-2-acetic acid (+-)-9h-carbazole-2-aceticaci c5720 carprofeno dl-6-chloro-alpha-methylcarbazole-2-aceticacid imadyl rimadyl D-(+)-GLUCOSE SOLUTION (45%) CELL*CULTUR E TESTED Carprofen, 98%, a COX2 inhibitor kanujofen Caroline Carprofen Standard Carprofen CRS Carprofen for system suitability CRS Carprofen > Ridamyl (2RS)-2-(6-Chloro-9H-carbazol-2-yl)propanoic acid 2-(6-chloro-9H-carbazol-2-yl)-3,3,3-trideuteriopropanoic acid Carprofen USP/EP/BP Carprofen-13C,d3 CarprofenQ: What is Carprofen Q: What is the CAS Number of Carprofen Carprofen (Y0000846) (+/-)-6-chloro-alpha-methylcarbazole-2-acetic acid Carprofen (1096699) chloro-alpha-methylcarbazole 2-(6-Chloro-carbazol-2-yl)-propionic acid Pregabalin Impurity 87 Carprofen EP/USP Ridamyl|||Imadyl|||Rimadyl 53716-49-7 3716-49-7 C15H12ClNO2 API RIMADYL Intermediates & Fine Chemicals Pharmaceuticals Active Pharmaceutical Ingredients Heterocycles Heterocyclic Compounds