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Balsalazide

Product Name
Balsalazide
CAS No.
80573-04-2
Chemical Name
Balsalazide
Synonyms
Giazo;CS-1360;balsalazido;BALSALAZIDE;Balsalazine;Balsalazidum;COLAZAL;GIAZO;Balsalazide D4;BALSALAZIDE SODIUM;BALSALZIDE DISODIUM
CBNumber
CB9148828
Molecular Formula
C17H15N3O6
Formula Weight
357.32
MOL File
80573-04-2.mol
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Balsalazide Property

Melting point:
254-255?C
Boiling point:
729.6±60.0 °C(Predicted)
Density 
1.44±0.1 g/cm3(Predicted)
vapor pressure 
0Pa at 20℃
storage temp. 
-20°C Freezer
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
2.97±0.10(Predicted)
color 
Yellow to Beige
LogP
1 at 25℃ and pH7.5
EPA Substance Registry System
Benzoic acid, 5-[(1E)-2-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]diazenyl]-2-hydroxy- (80573-04-2)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
18680
Product name
Balsalazide
Purity
≥98%
Packaging
5mg
Price
$57
Updated
2024/03/01
Cayman Chemical
Product number
18680
Product name
Balsalazide
Purity
≥98%
Packaging
10mg
Price
$107
Updated
2024/03/01
Cayman Chemical
Product number
18680
Product name
Balsalazide
Purity
≥98%
Packaging
25mg
Price
$233
Updated
2024/03/01
Cayman Chemical
Product number
28888
Product name
Balsalazide-d4
Packaging
1mg
Price
$396
Updated
2024/03/01
Cayman Chemical
Product number
18680
Product name
Balsalazide
Purity
≥98%
Packaging
50mg
Price
$437
Updated
2024/03/01
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Balsalazide Chemical Properties,Usage,Production

Description

Colazide was launched in the UK for mild to moderate acute attacks of ulcerative colitis. It can be prepared by diazotization of 3-(4-aminobenzoylamino) propionic acid followed by condensation with salicylic acid. Colazide, an analogue of sulfasalazine, was found to be non-toxic and non-mutagenic in the Ames test. Once ingested the molecule releases a non-toxic fragment, 4-aminobenzoyl-β-alanine (poorly absorbed - 75% excretion in stool), and the active component 5- aminosalicylic acid (Mesalazine). The exact mechanism of action is not clearly understood but it is cytoprotective and has antiinflammatory properties. Other biological effects have been observed and include the following: (a) granulocyte activation is blocked, (b) there is a reduction in myeloperoxidase activity, and (c) a reduction in the release of arachidonic acid with a concomitant decrease in prostaglandin and leucotriene (as indicated by the lack of production of LTB4) production. It can behave as a reactive oxygen species (ROS) scavenger, inhibit PAF formation, reduce IL-1 production, and antagonize TNF and NK cells. While comparable in efficacy to sulfasalazine, Colazide removes the possibility of sulfasalazine side-effects, such as, agranulocytosis, hepatotoxicity and male infertility.

Description

Balsalazide is a prodrug form of 5-aminosalicylic acid (5-ASA; ). It is cleaved by bacterial azoreductases in the intestinal lumen to release 5-ASA. Balsalazide (600 mg/kg per day) decreases IL-2 levels and increases IL-6 levels in the serum and colonic mucosa membrane, as well as decreases micro- and macroscopic colonic damage, in a rat model of colitis induced by 2,4-dinitrochlorobenzene (DNCB). Formulations containing balsalazide have been used in the treatment of ulcerative colitis.

Chemical Properties

Yellow Solid

Originator

Biorex (UK)

Uses

An analogue of Sulfasalazine, A prodrug of 5-Aminosalicylic Acid

Uses

Balsalazide-d4 is an isotopically labelled analog of Balsalazide (B116300), which is an analogue of Sulfasalazine (S699084). A prodrug of 5-aminosalicylic acid where carrier molecule is 4-aminobenzoyl-β-alanine. Anti-inflammatory (gastrointestinal).

Definition

ChEBI: A monohydroxybenzoic acid consisting of 5-aminosalicylic acid (mesalazine) linked to 4-aminobenzoyl-beta-alanine via an azo bond.

Manufacturing Process

125 g finely powdered 4-nitrobenzoyl chloride were added portionwise, while stirring, to a solution of 70 g β-alanine in 500 ml water containing 65 g sodium hydroxide and cooled to 5°C. The reaction mixture was stirred for 3 hours and then added to a mixture of ice and hydrochloric acid. The precipitate obtained was filtered off, washed with water and dried by suction. After crystallisation of the dried product from hot acetone, there were obtained 130 g 4-nitrobenzoyl-β-alanine, M.P. 164°-166°C.
A suspension of 15 g finely powdered 4-nitrobenzoyl-β-alanine in 200 ml ethanol was stirred in an atmosphere of hydrogen in the presence of 1 g of palladium-charcoal (5%), while cooling gently. When the absorption of hydrogen had ceased, the reaction mixture was filtered and the filtrate concentrated to a small volume. Upon adding diethyl ether and cooling 4- aminobenzoyl-β-alanine was obtained. The yield was 11.5 g, M.P. 156°-158°C.
8.8 g 4-aminobenzoyl-β-alanine were triturated with 12 ml hydrochloric acid and the paste obtained was dissolved in 100 ml water. The solution was cooled to -5°C and a solution of 3 g sodium nitrite in 20 ml water, cooled to 0°C, was added dropwise, while stirring. The diazotised solution was left for 1 hour at 0°C and was then added dropwise at -5°C to a solution of 6 g salicylic acid in 70 ml water containing 3.6 g sodium hydroxide and 7 g sodium carbonate. The final reaction mixture was adjusted to a pH of about 8, stirred for 2 to 3 hours and added to a mixture of dilute hydrochloric acid and ice. The precipitate obtained was filtered off, washed with water and suction dried. Crystallisation from hot ethanol gave 11.9 g 5-[(2-carboxy-ethylcarbamoyl)- phenylazo]-2-hydroxy-benzoic acid, M.P. 254°-255°C.
10.7 g of the free acid were dissolved in 300 ml warm ethanol and treated with a solution of 2.4 g sodium hydroxide in 25 ml ethanol. The precipitate obtained was filtered off, washed with ethanol and diethyl ether and dried in a vacuum at 50°C to give 11.5 g of the disodium salt of 5-[(2-carboxyethylcarbamoyl)- phenylazo]-2-hydroxy-benzoic acid, M.P. >350°C.

brand name

Colazal (Salix).

Therapeutic Function

Antiinflammatory

Clinical Use

Treatment and maintenance of remission, in mild to moderate ulcerative colitis

Metabolism

Very little of an oral dose of balsalazide is absorbed via the upper gastrointestinal tract, and almost the entire dose reaches its site of action in the colon intact. It is broken down by the colonic bacterial flora into 5-aminosalicylic acid (mesalazine), which is active, and 4-aminobenzoylalanine, which is considered to be an inert carrier. Most of a dose is eliminated via the faeces, but about 25% of the released mesalazine is absorbed and acetylated. A small proportion of 4-aminobenzoylalanine is absorbed and acetylated by first-pass metabolism through the liver. The acetylated metabolites are excreted in the urine.

Balsalazide Preparation Products And Raw materials

Raw materials

Preparation Products

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Balsalazide Suppliers

Carbosynth
Tel
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Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
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Apin Chemicals Limited (UK)
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Email
info@apinchemicals.com
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United Kingdom
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6184
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Leancare Ltd.
Tel
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Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
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42
MOLEKULA Ltd.
Tel
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Fax
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Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
CARBONE SCIENTIFIC CO.,LTD
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Email
sales@carbonesci.com
Country
United Kingdom
ProdList
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Eurolabs Limited
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Country
United Kingdom
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6309
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ETA SCIENTIFIC Co.,Ltd
Tel
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Email
sales@etascientific.com
Country
United Kingdom
ProdList
6090
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34
UK GREEN SCIENTIFIC CO.,LIMITED
Tel
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Email
sales@gs-chem.com
Country
United Kingdom
ProdList
6098
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Sequoia Research Products Ltd.
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sales@seqchem.com
Country
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View Lastest Price from Balsalazide manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
Balsalazide 80573-04-2
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10
Zhuozhou Wenxi import and Export Co., Ltd
Product
Balsalazide 80573-04-2
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-08
Career Henan Chemical Co
Product
Balsalazide 80573-04-2
Price
US $1.00/KG
Min. Order
1G
Purity
98%
Supply Ability
100KG
Release date
2018-08-20

80573-04-2, BalsalazideRelated Search:


  • 5-((4-(((2-carboxyethyl)amino)carbonyl)phenyl)azo)-2-hydroxy-benzoicaci(e
  • BALSALZIDE DISODIUM
  • BALSALAZIDE SODIUM
  • BALSALAZIDE
  • balsalazido
  • BALSALAZIDE DISODIUM SALT
  • (E)-5-[[4-[[(2-Carboxyethyl)amino]-carbonyl]phenyl]azo-2-hydroxybenzoic acid
  • Benzoic acid, 5-((1E)-(4-(((2-carboxyethyl)amino)carbonyl)phenyl)azo)-2-hydroxy-
  • Benzoic acid, 5-((4-(((2-carboxyethyl)amino)carbonyl)phenyl)azo)-2-hydroxy-, (E)-
  • 5-[(1E)-2-[4-[[(2-Carboxyethyl)aMino]carbonyl]phenyl]diazenyl]-2-hydroxybenzoic Acid
  • Balsalazide D4
  • (E)-5-((4-((2-Carboxyethyl)carbamoyl)phenyl)diazenyl)-2-hydroxybenzoic acid
  • COLAZAL;GIAZO
  • Giazo
  • Balsalazine
  • CS-1360
  • Benzoic acid, 5-[(1E)-2-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]diazenyl]-2-hydroxy-
  • Balsalazide D4Q: What is Balsalazide D4 Q: What is the CAS Number of Balsalazide D4 Q: What is the storage condition of Balsalazide D4 Q: What are the applications of Balsalazide D4
  • Balsalazidum
  • 80573-04-2
  • 80573-04-02
  • C17H15N3O6
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