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(S)-Flurbiprofen

CAS No.
51543-39-6
Chemical Name:
(S)-Flurbiprofen
Synonyms
Esflurbiprofen;(S)-2-Flurbiprofen;CS-1959;C1sH13FO2;d-Flurbiprofen;Dexflurbiprofen;(S)-FLURBIPROFEN;(+)-Flurbiprofen;(S)-(+)-FLURBIPROFEN;Flurbiprofen (S)-Isomer
CBNumber:
CB8284910
Molecular Formula:
C15H13FO2
Molecular Weight:
244.26
MDL Number:
MFCD00866152
MOL File:
51543-39-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

(S)-Flurbiprofen Properties

Melting point 109-110 °C(lit.)
Boiling point 376.2±30.0 °C(Predicted)
Density 1.199±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility insoluble in H2O; ≥10.9 mg/mL in DMSO; ≥69.1 mg/mL in EtOH
form A crystalline solid
pka 4.14±0.10(Predicted)
color White to off-white
InChI InChI=1/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)/t10-/s3
InChIKey SYTBZMRGLBWNTM-JQHDBZEONA-N
SMILES C1(=CC=C([C@H](C)C(=O)O)C=C1F)C1=CC=CC=C1 |&1:4,r|
FDA UNII J5ZZK9P7MX
ATC code M02AA29

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310+P330-P405-P501
Hazard Codes  T
Risk Statements  25
Safety Statements  36/37/39-45
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
NFPA 704
0
2 0

(S)-Flurbiprofen price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 10004207 (S)-Flurbiprofen ≥99% 51543-39-6 100mg $107 2026-04-30 Buy
Cayman Chemical 10004207 (S)-Flurbiprofen ≥99% 51543-39-6 250mg $255 2026-04-30 Buy
Cayman Chemical 10004207 (S)-Flurbiprofen ≥99% 51543-39-6 500mg $481 2026-04-30 Buy
Cayman Chemical 10004207 (S)-Flurbiprofen ≥99% 51543-39-6 1g $854 2026-04-30 Buy
ChemScene CS-0003779 (S)-Flurbiprofen 99.88% 51543-39-6 100mg $81 2026-06-04 Buy
Product number Packaging Price Buy
10004207 100mg $107 Buy
10004207 250mg $255 Buy
10004207 500mg $481 Buy
10004207 1g $854 Buy
CS-0003779 100mg $81 Buy

(S)-Flurbiprofen Chemical Properties, Uses, Production

Description

Marketed by Taisho Pharmaceutical Holdings Co., Ltd., and Teijin Pharma Ltd., the (S)-enantiomer of flurbiprofen (named Esflurbiprofen) was approved as a new drug by the PMDA of Japan in 2015. (S)- Flurbiprofen, a cyclooxygenase (COX)-inhibiting nonsteroidal anti-inflammatory (NSAID) drug, is formulated with mentha oil and administered by way of a patch as a treatment for osteoarthritis in the current invention. Interestingly, the (R)- enantiomer is responsible for minimal COX inhibition but has been implicated as a possible treatment for a variety of other diseases. Synthetic approaches to racemic flurbiprofen have been reported in the chemical literature as early as the 1960s, and the mixture was approved as a drug in the United States by the FDA in 1988, marketed by Pharmacia and Upjohn. Toward this end, the current patent estate defines the utility of the active S-enantiomer, and synthetic approaches therein apply to this enantiomer only.

Description

(S)-Flurbiprofen is the COX-active enantiomer of the non-selective COX inhibitor flurbiprofen with IC50 values of 0.48 and 0.47 μM for COX-1 and COX-2, respectively, in guinea pig whole blood. It inhibits the release of 6-keto prostaglandin F (6-keto-PGF; ) and thromboxane B2 (TXB2; ) from rat whole blood, gastric mucosa, lung, and jejunal tissue ex vivo in a dose-dependent manner. (S)-Flurbiprofen (1 nM) inhibits basal and bradykinin-, serotonin-, and histamine-stimulated prostaglandin E2 (PGE2) release from isolated skin flaps of rat lower hind paws. It also inhibits release of the neuroinflammatory marker calcitonin gene-related peptide (CGRP; Item Nos. 24405 | 24725 | 24728) when used at a concentration of 1 μM. In vivo, (S)-flurbiprofen reduces the number of flinches per minute in the formalin test in rats, indicating antinociceptive activity.

Uses

(S)-Flurbiprofen is the S-isomer of Flurbiprofen (F598700), an anti-inflammatory used as an analgesic.

Definition

ChEBI: (S)-flurbiprofen is a flurbiprofen. It is an enantiomer of a (R)-flurbiprofen.

Synthesis

The synthesis began with conversion of commercially available aniline 168 to racemic flurbiprofen (169) through a Sandmeyer reaction and subsequent phenyl group introduction through the use of sodium tetraphenylborate. A chiral resolution was then performed on the resulting stereogenic acid on multikilogram scale by treatment with (S)- 1-phenylethylamine in MeOH/toluene, which gave various yields of salt 170 as reported by the authors. Acidification with aqueous HCl delivered (S)-flurbiprofen (XXI). Importantly, with respect to green chemistry considerations, the (R)- enantiomer could be recycled by racemizing the undesired (R)- enantiomer 171 in refluxing methanolic sulfuric acid, improving the overall atom economy of the process and significantly reducing waste.

Synthesis_51543-39-6

in vitro

it was found that the ic50 value of (s)-flurbiprofen was about 0.5 μm for both cox-1 and cox-2 in guinea pig whole blood [1].

in vivo

the efficacy of multiple applications of s(+)-flurbiprofen plaster (sfpp) was evaluated for the alleviation of inflammatory pain and edema in rat adjuvant-induced arthritis model. multiple applications of sfpp could exert a significant analgesic effect from the first day of application as compared to the other nsaid drugs. in terms of paw edema, sfpp could decrease edema from the second day after application. moreover, multiple applications of sfpp were found to be superior to those of other nsaid drugs in terms of the analgesic effect [2].

IC 50

0.5 μm for both cox-1 and cox-2 in guinea pig whole blood

References

[1] barnett, j. ,chow, j.,ives, d., et al. purification, characterization and selective inhibition of human prostaglandin g/h synthase 1 and 2 expressed in the baculovirus system. biochimica et biophysica acta 1209, 130-139 (1994).
[2] sugimoto m et al. topical anti-inflammatory and analgesic effects of multiple applications of s(+)-flurbiprofen plaster (sfpp) in a rat adjuvant-induced arthritis model. drug dev res. 2016 jun;77(4):206-11.
[3] yataba i, otsuka n, matsushita i, matsumoto h, hoshino y. the efficacy and safety of s-flurbiprofen plaster in the treatment of knee osteoarthritis: a phase ii, randomized, double-blind, placebo-controlled, dose-finding study. j pain res. 2017 apr 11;10:867-880.

(S)-Flurbiprofen Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 170)
Supplier Tel Email Country ProdList Advantage
Chengdu Senior Pharma Technology Co.Ltd. +86-0838-2319818 +86-15982001943 seniorpharma@163.com China 460 55
Pushan Industry (Shaanxi) Co., Ltd. 029-81310890 18165209495 2929288192@qq.com China 9949 58
Shaoxing Hongda Medical Technology Co.,Ltd 18072995930 sales001@hongdabova.com China 26 58
Hunan Eurasian Pharmaceutical Co. Ltd. 0592-5789919 13328776692 2851802018@qq.com;2851802016@qq.com China 88 58
Beijing Jingzi Pharmaceutical Technology Co., Ltd. 15011485209 17241816@qq.com China 79 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Nanjing Chemlin Chemical Co., Ltd 025-83697070 13770331960 info@chemlin.com.cn China 16305 64
Daicel Chiral Technologies (China)CO.,LTD 021-50460086-9 15921403865 han_yajun@dctc.daicel.com China 7909 65
Tianjin heowns Biochemical Technology Co., Ltd. 400 638 7771 sales@heowns.com China 14412 57
Maya High Purity Chemicals +86 (573) 82222445 (0)18006601000 452520369 sales@maya-r.com China 11693 57

View Latest Price from (S)-Flurbiprofen manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Esflurbiprofen pictures 2026-08-25 Esflurbiprofen
51543-39-6
$1.10-9.90 1kg 99%min 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
(S)-Flurbiprofen USP/EP/BP pictures 2026-08-20 (S)-Flurbiprofen USP/EP/BP
51543-39-6
$1.10 1g 99.9% 100 Tons Min Dideu Industries Group Limited
(S)-Flurbiprofen pictures 2026-07-27 (S)-Flurbiprofen
51543-39-6
$29.00 99.99% 10g TargetMol Chemicals Inc.
  • Esflurbiprofen pictures
  • Esflurbiprofen
    51543-39-6
  • $1.10-9.90
  • 99%min
  • ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD

(S)-Flurbiprofen Spectrum

(S)-(+)-FLURBIPROFEN (S)-FLURBIPROFEN (S)-(+)-2-FLUORO-ALPHA-METHYL-4-BIPHENYLACETIC ACID (S)-2-fluoro-alpha-methyl[1,1'-biphenyl]-4-acetic acid (S)-(+)-2-Fluoro-α-methyl-4-biphenylacetic acid [1,1'-Biphenyl]-4-acetic acid, 2-fluoro-α-methyl-, (S)- [1,1'-Biphenyl]-4-acetic acid, 2-fluoro-α-methyl-, (αS)- d-Flurbiprofen (S)-2-(2-Fluoro-1,1'-biphenyl-4-yl)propionic acid (S)-3-Fluoro-α-methyl-4-phenylbenzeneacetic acid (S)-(+)-2-Fluoro-alpha-methyl-4-biphenylacetic acid (Flurbiprofe 2S)-2-(2-Fluoro-4-biphenyl)propanoic acid Dexflurbiprofen (S)-(+)-2-FLUORO-ALPHA-METHYL-4-BIPHENYLACETIC ACID (FLURBIPROFEN) [1,1'-Biphenyl]-4-aceticacid, 2-fluoro-a-methyl-,(aS)- (S)-2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanoic acid BTS-24332,SFPP,TT-063,Esflurbiprofen (S)-2-(2-Fluorobiphenyl-4-yl)propanoic acid CS-1959 Flurbiprofen (S)-Isomer (S)-Flurbiprofen USP/EP/BP CS-O-34753Q: What is CS-O-34753 Q: What is the CAS Number of CS-O-34753 (S)-Flurbiprofen,Esflurbiprofen (+)-Flurbiprofen Prostaglandin E synthase,PGE synthase,Cyclooxygenase,COX,(S)-Flurbiprofen,(S) Flurbiprofen,Inhibitor,inhibit,(S)Flurbiprofen C1sH13FO2 (S)-2-(2-Fluoro-4-biphenylyl)propanoic Acid Flurbiprofen Impurity 129 (S)-2-Flurbiprofen Esflurbiprofen 51543-39-6 C15H13O2F C6H5C6H3FCHCH3CO2H Chiral Building Blocks Asymmetric Synthesis Carboxylic Acids Organic Building Blocks