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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
Molecular Weight:
357.32
MDL Number:
MFCD00868204
MOL File:
80573-04-2.mol
MSDS File:
SDS
Last updated:2023-05-18 11:31:16

Balsalazide Properties

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
EWG's Food Scores 1
FDA UNII P80AL8J7ZP
ATC code A07EC04
EPA Substance Registry System Benzoic acid, 5-[(1E)-2-[4-[[(2-carboxyethyl)amino]carbonyl]phenyl]diazenyl]-2-hydroxy- (80573-04-2)

Pharmacokinetic data

Protein binding 40 (similar to mesalazine), (NASA - 80%)
Excreted unchanged in urine 25 (as metabolites)

Balsalazide price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18680 Balsalazide ≥98% 80573-04-2 5mg $57 2024-03-01 Buy
Cayman Chemical 18680 Balsalazide ≥98% 80573-04-2 10mg $107 2024-03-01 Buy
Cayman Chemical 18680 Balsalazide ≥98% 80573-04-2 25mg $233 2024-03-01 Buy
Cayman Chemical 28888 Balsalazide-d4 80573-04-2 1mg $396 2024-03-01 Buy
Cayman Chemical 18680 Balsalazide ≥98% 80573-04-2 50mg $437 2024-03-01 Buy
Product number Packaging Price Buy
18680 5mg $57 Buy
18680 10mg $107 Buy
18680 25mg $233 Buy
28888 1mg $396 Buy
18680 50mg $437 Buy

Balsalazide Chemical Properties,Uses,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

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).

Uses

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

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

Global( 174)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
Baoji Guokang Bio-Technology Co., Ltd.
0917-3909592 13892490616 gksales1@gk-bio.com China 9339 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118 xie@china-sinoway.com China 992 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418684 +8618949823763 sales@tnjchem.com China 25363 58

View Lastest Price from Balsalazide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Balsalazide pictures 2023-04-20 Balsalazide
80573-04-2
US $50.00 / kg 1kg 99% 100 tons Hebei Duling International Trade Co. LTD
Balsalazide pictures 2021-07-13 Balsalazide
80573-04-2
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
Balsalazide pictures 2021-07-09 Balsalazide
80573-04-2
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • Balsalazide pictures
  • Balsalazide
    80573-04-2
  • US $50.00 / kg
  • 99%
  • Hebei Duling International Trade Co. LTD
  • Balsalazide pictures
  • Balsalazide
    80573-04-2
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd
  • Balsalazide pictures
  • Balsalazide
    80573-04-2
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd

Balsalazide Spectrum

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 API Amines Aromatics Intermediates & Fine Chemicals Pharmaceuticals Active Pharmaceutical Ingredients