High Quality CAS 5104-49-4 Flurbiprofen For Analgesic

Details:

What's Flurbiprofen Powder

Product Name	Flurbiprofen
CAS:	5104-49-4
MF:	C15H13FO2
Appearance	White to light yellow crystal powder
Molecular Weight	244.26
EINECS:	225-827-6

Flurbiprofen synthesis was originally reported in 1974. During a study of the pharmacological properties

of a large number of substituted phenylalkanoic acids, including ibuprofen and ibufenac, the most potent

were found to be substituted 2-(4-biphenyl)propionic acids. Further toxicological and pharmacological

studies indicated that flurbiprofen possessed the most favorable therapeutic profile, so it was selected

for further clinical development. It was not marketed until 1987, when it was introduced as the sodium

salt as Ocufen, the first topical NSAID indicated for ophthalmic use in the United States. The indication

for Ocufen is the same as that for Profenal-that is, to inhibit intraoperative miosis induced by

prostaglandins in cataract surgery.

 

 

Application & Function 

1.

(1) Prevention of ophthalmologic cystic edema after removal of crystals.

(2) Treatment of anterior segment inflammation after cataract and trabecular argon laser surgery.

(3) Inhibition of pupil contraction during surgery.

2. Clinically used to inhibit pupil dilation and postoperative anti-inflammatory during endoscopic surgery.

Treatment of inflammatory response after laser trabeculectomy and other inflammatory reactions

in the anterior segment of the eye. It also has a therapeutic effect on contact lens-induced giant

papillary conjunctivitis, anterior uveitis and cystoid macular edema.

3. For rheumatoid arthritis.

 

   

Items		Standards	Results
Appearance	White or off-white powder		Off-white powder
Identification	By HPLC		Complies
Melting Point	120ºC~130ºC		126ºC
Loss on Drying	≤1.00%		0.21%
Heavy Metals	≤ 10ppm		Complies
Sulfated Ash	≤ 0.10%		0.03%
Chlorine Content	17.5%~19.5%		19.3%
Arsenic Content	≤ 0.1ppm		0.09ppm
Lead VContent	≤ 3.0ppm		0.50ppm
Cadmium Content	≤ 0.1ppm		0.10ppm
Mercury Content	≤ 0.1ppm		0.10ppm
Microbiological Test	Coliforms:Negative		Negative
	Salmonella: Negative		Complies
	Total plate count: ≤1000 CFU/g		Pass
	Yeast&Mold: ≤50 CFU/g		Pass
Related Substances	Impurity A: ≤0.30%		0.18%
	Other unknown impurity: ≤0.10%		0.07%
	Total Impurities: ≤0.50%		0.42%
Assay	≥ 98.0%		99.50%
Reference Standard	USP Standard
Conclusion	The product complied to USP standard.
Storage	Preserve in tight,light-resistant containers in a cool place

 

 

1. All inquiries will be replied within 12 hours.

2. Dedication to quality, supply & service.

3. Strictly on selecting raw materials.

4. OEM/ODM Available.

5. Reasonable & competitive price, fast lead time.

6. Sample is available for your evaluation & Formulation development.

7. Faster delivery:Sample order in stock and 3-7 days for bulk production.

8.We have strong cooperation with DHL, TNT, UPS, FEDEX, EMS. Or you also can choose your own shipping forwarder

9. After-Sale Service:
1) International Authorized Third-Party Test For The Products You Demand.

2) 30 Days Warranty of quality of goods. 

 

Delivery & Payment Terms

Julong Bio-Tech Co., Ltd. is located in Xi'an City, Shaanxi Province, China. It is a biotechnology enterprise engaged

in the research, development, production and sales of animal and plant extracts, cosmetics, pharmaceutical raw materials

and intermediates. The company has complete experimental facilities. And advanced testing instruments ensure the stability

of product quality from all aspects. The company has a complete sales service system, the products are exported to countries

all over the world, and have won a good international reputation with excellent quality and excellent service.

The company has been adhering to the basic principles of "integrity, quality, service, and win-win" to serve customers,

constantly strict requirements, set goals, and implement win-win development.

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