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Bromfenac sodium

Product Name
Bromfenac sodium
CAS No.
91714-94-2
Chemical Name
Bromfenac sodium
Synonyms
Xibrom;Yellox;BROMFENAC;AHR 10282;Bromfenaco;Bromofenac;AKOS 91023;Bromfenacum;Unii-864p0921dw;Bromfenacum [latin]
CBNumber
CB8117032
Molecular Formula
C15H12BrNO3
Formula Weight
334.16
MOL File
91714-94-2.mol
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Bromfenac sodium Property

Boiling point:
562.2±50.0 °C(Predicted)
Density 
1.565±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
4.07±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
A594895
Product name
2-(2-Amino-3-(4-bromobenzoyl)phenyl)aceticAcid
Packaging
50mg
Price
$60
Updated
2021/12/16
TRC
Product number
A594895
Product name
2-(2-Amino-3-(4-bromobenzoyl)phenyl)aceticAcid
Packaging
200mg
Price
$155
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB66513
Product name
Bromfenac
Packaging
100mg
Price
$150
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB66513
Product name
Bromfenac
Packaging
25mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0009095
Product name
BROMFENAC
Purity
95.00%
Packaging
250MG
Price
$222.6
Updated
2021/12/16
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Bromfenac sodium Chemical Properties,Usage,Production

Originator

Duract,Wyeth-Ayerst

Uses

Analgesic.

Uses

Bromfenac (Xibrom, ISTA Pharmaceuticals, Irvine, USA; Bronuck, Senju Pharmaceutical, Osaka, Japan) is indicated for the treatment of postoperative inflammation and the reduction of ocular pain in patients after undergoing cataract extraction. For this task, one drop of Xibrom may be applied to the affected eye twice daily beginning 24 hours after cataract surgery and continuing for the first 2 weeks of the postoperative period. The clinical safety and efficacy of bromfenac have been extensively studied in diverse comparative investigations, including the treatment of external or anterior ocular inflammatory diseases, allergic conjunctivitis, scleritis, and postoperative inflammation.The results of two phase III multicenter, randomized double-masked placebo-controlled clinical trials showed that bromfenac ophthalmic solution 0.09% was effective in the rapid resolution of ocular pain after cataract surgery, and there was a statistically significant difference between the bromfenac and placebo groups demonstrated in these phase III clinical trials.

Definition

ChEBI: Amfenac in which the the hydrogen at the 4 position of the benzoyl group is substituted by bromine. It is used for the management of ocular pain and treatment of postoperative inflammation in patients who have undergone cataract extraction. It was withdraw from the US market in 1998, following concerns over off-label abuse and hepatic failure.

Manufacturing Process

Reaction of (2-aminophenyl)-(4-bromophenyl)-methanone with methylsulfanylacetic acid ethyl ester and tert-butyl hypochlorite gives a corresponding sulfonium salt. This salt was transformed to initially to the betaine. Electrocyclic rearrangement of that transient intermediate leads, after rearomatization, to the homoanthranilic acid. Internal ester-amine interchange leads then to 4-bromophenyl-(3-(methylthio)indolin-7-yl)methanone. The thiomethyl group is then removed with Raney nickel to give 4-bromophenyl- (indolin-7-yl)methanone. Saponification of this intermediate affords the (2- amino-3-(4-bromobenzoyl)-phenyl)-acetic acid (Bromfenac).
In practice it is usually used as sodium salt.

brand name

Xibrom (Ista).

Therapeutic Function

Analgesicá Antiinflammatory

Pharmacology

The drug is rapidly absorbed and excreted. The drug’s long duration of anti-inflammatory action despite its short half-life deserves further investigation.

Clinical Use

Bromfenac, used as the sodium salt, is a non-steroidal anti-inflammatory drug acting via inhibition of COX-1 and COX-2. It was launched in Japan in 2000 by Senju for topical treatment of ocular inflammation and has been approved in the United States in 2006 for the treatment of pain following cataract surgery. It was used for the short-term treatment of acute pain, but it was withdrawn for this indication in June 1998 because of several postmarketing reports of severe hepatic failure

Synthesis

The cyclization of 2-amino-4’- bromobenzophenone with ethyl 2-(methylthio) acetate with tert-butyl hypochlorite as catalyst in dichloromethane at 70 ?C gives 7- (4-bromobenzoyl)-3-(methylthio)-2,3-dihydro- 1H-indol-2-one, which is desulfurized by treatment with Raney nickel in THF yielding 7-(4- bromobenzoyl)-2,3-dihydro-1H-indol-2-one. Finally, this compound is hydrolyzed with refluxing 3 M aqueous NaOH and acidified with concentrated HCl .

Veterinary Drugs and Treatments

Bromfenac is a nonsteroidal anti-inflammatory drug (NSAID) by virtue of its ability to block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2. Bromfenac is indicated for treatment of postoperative inflammation in patients who have undergone cataract extraction.

Bromfenac sodium Preparation Products And Raw materials

Raw materials

Preparation Products

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Bromfenac sodium Suppliers

Nanjing Endesa Bio-tech Co., Ltd.
Tel
025-58862853 18915922038
Fax
+86-025-58862853
Email
sales@endesachem.com
Country
China
ProdList
591
Advantage
58
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Fax
0573-85285100
Email
isenchem@163.com
Country
China
ProdList
9413
Advantage
66
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
19172
Advantage
64
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
021-51613915-820 13611835272
Fax
021 51613951
Email
mmwang@sunwaypharm.cn
Country
China
ProdList
9734
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4552
Advantage
62
S.Z. PhyStandard Bio-Tech. Co., Ltd.
Tel
0755-83725681-603
Fax
+86 755 28094224
Country
China
ProdList
4496
Advantage
50
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
Chengdu AstaTech Trading Co., Ltd./AstaTech (Chengdu) Pharma. Co., Ltd.
Tel
+86-28-85122536 85324413
Fax
+86-28-85326443
Email
market@astatech.cn
Country
China
ProdList
8026
Advantage
55
ALPENGLOW CHEMICAL INDUSTRIAL CO., LTD
Tel
086-0531-86986713
Fax
086-0531-86980810
Email
aplgroup@163.com
Country
China
ProdList
96
Advantage
58
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
18042
Advantage
56
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View Lastest Price from Bromfenac sodium manufacturers

Career Henan Chemical Co
Product
bromfenac 91714-94-2
Price
US $8.80/KG
Min. Order
1KG
Purity
97%-99%
Supply Ability
100kg
Release date
2019-07-10

91714-94-2, Bromfenac sodiumRelated Search:


  • BROMFENAC
  • 2-Amino-3-(4-bromobenzoyl)benzeneacetic acid
  • Bromofenac
  • Benzeneacetic acid, 2-amino-3-(4-bromobenzoyl)-
  • Bromfenaco
  • Bromfenaco [spanish]
  • Bromfenacum
  • Bromfenacum [latin]
  • Unii-864p0921dw
  • Xibrom
  • 2-(2-AMino-3-(4-broMobenzoyl)phenyl)acetic acid
  • AKOS 91023
  • Yellox
  • [2-Amino-3-(p-bromobenzoyl)phenyl]acetic acid
  • AHR 10282
  • 2-(2-Amino-3-(4-bromobenzoyl)
  • 91714-94-2
  • C15H11BrNNaO3
  • C15H12BrNO3
  • Miscellaneous