Y0002271

Flurbiprofen for peak identification

CRS, European Pharmacopoeia (EP) Reference Standard

Manufacturer: Sigma Aldrich

CAS Number: 5104-49-4

Synonym(S): Flurbiprofen, (±)-2-Fluoro-α-methyl-4-biphenylacetic acid, L-790,330

Select a Size

Pack Size SKU Availability Price
20 MG Y0002271-20-MG In Stock ₹ 16,984.43

Y0002271 - 20 MG

₹ 16,984.43

In Stock

Quantity

1

Base Price: ₹ 16,984.43

GST (18%): ₹ 3,057.197

Total Price: ₹ 20,041.627

API family

flurbiprofen

manufacturer/tradename

EDQM

mp

110-112 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(C(O)=O)c1ccc(c(F)c1)-c2ccccc2

InChI

1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)

InChI key

SYTBZMRGLBWNTM-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
50-196-8298
Medchemexpress LLC HY-10582 100mg Medchemexpress, Flurbiprofen CAS:5104-49-4 Purity:>98%
Medchemexpress LLC ₹ 5,929.31
PHR1499
Flurbiprofen
Supelco ₹ 12,935.88
1285750
Flurbiprofen
Sigma Aldrich ₹ 40,756.13
F0285200
Flurbiprofen
Sigma Aldrich ₹ 16,107.60
F8514
Flurbiprofen
Sigma Aldrich ₹ 9,731.68 - ₹ 94,458.95
F8514
Flurbiprofen
Sigma Aldrich ₹ 9,731.68 - ₹ 94,458.95
CS-2208
Flurbiprofen
ChemScene ₹ 1,540.08 - ₹ 17,454.24
AB74266
5104-49-4 | Flurbiprofen
A2B Chem ₹ 770.04 - ₹ 22,502.28

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Description

  • General description: This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
  • Application: Flurbiprofen for peak identification EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
  • Biochem/physiol Actions: Fluibiprofen is a cyclooxygenase (COX) inhibitor, which is an enzyme responsible for the conversion of arachidonic acid to prostaglandin G2 (PGG2) and PGG2 to prostaglandin H2 (PGH2) in the prostaglandin synthesis pathway. This decreases the prostaglandins which cause inflammation, pain, swelling and fever. Flurbiprofen inhibits the activity of both COX-1 and -2. The S enantiomer inhibits prostaglandin synthesis and has both anti-inflammatory and analgesic activity, while the R enantiomer does not inhibit prostaglandin synthesis and displays only analgesic activity.
  • Packaging: The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
  • Other Notes: Sales restrictions may apply.

SAFETY INFORMATION

Pictograms

GHS06

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 3 Oral

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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CC(C(O)=O)c1ccc(c(F)c1)-c2ccccc2

InChI:
1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)

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SYTBZMRGLBWNTM-UHFFFAOYSA-N

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1S/C22H31NO3.ClH/c1-3-23(4-2)17-11-12-18-26-21(24)22(25,19-13-7-5-8-14-19)20-15-9-6-10-16-20;/h5,7-8,13-14,20,25H,3-4,6,9-10,15-18H2,1-2H3;1H

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SWIJYDAEGSIQPZ-UHFFFAOYSA-N

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