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Mesalamine

CAS 89-57-6C7H7NO3MW 153.14

Mesalamine (CAS 89-57-6) — formula C7H7NO3, molecular weight 153.14.

Product Overview

CAS Number89-57-6
Molecular FormulaC7H7NO3
Molecular Weight153.14
Melting Point260-280 °C
LogP1.2
ApplicationsUses: Used to make dyes and light-sensitive paper, Also used as a gastrointestinal anti-inflammatory drug, [Merck Index] A metabolite of the drug sulfasalazine, [REPROTOX], In manufacture of light-sensitive paper, azo and sulfur dyes, Treatment of ulcerative colitis (England), It is used orally, in a delay-release formulation, as a retention enema, and as a suppository., THERAP CAT: Anti-inflammatory (gastrointestinal), Synthetic Polymer MALDI Matrix Compounds, Use (kg) in Switzerland (2009): >5000, Use (kg, approx.) in Germany (2009): >75000, exact) in Germany (2009): 96794, Use (kg) in USA (2002): 136000, Consumption (g per capita) in Switzerland (2009): 0.64, Consumption (g per capita, approx.) in Germany (2009): 0.92, exact) in Germany (2009): 1.2, Consumption (g per capita) in the USA (2002): 0.48, Excretion rate: 0.1, Calculated removal (%): 92.1, Use Classification: Pharmaceuticals, Methods of Manufacturing: Preparation by reduction of m-nitrobenzoic acid with Zn dust and HCl, Formulations, Preparations: ... The pharmaceutical industry has been developing different delivery systems for Multi-Matrix System (MMX) mesalamine for the treatment of Crohn's disease and ulcerative colitis. The new oral mesalamine formulation is a once-daily MMX tablet that delivers the mesalamine to the colon, making it most useful in the treatment of ulcerative colitis. The MMX coating matrix and coating system begin dissolution in the final portion of the ileum. ..., Oral: Capsules, extended-release: 250 mg Pentasa, (Shire), 500 mg Pentasa, (Shire). Tablets, delayed-release: 400 mg Asacol, (Procter & Gamble). Rectal: Suppositories: 500 mg Canasa, (Axcan Scandipharm), 1 g Canasa, (Axcan Scandipharm). Suspension: 4 g, 60 mL Mesalamine Suspension Enema, (Clay-Park), Mesalamine Suspension Enema, (Teva), Rowasa Suspension Enema (with potassium metabisulfite), (Solvay)., Oral: Tablet Delayed Release: 1.2 g Lialda (Shire)., Consumption Patterns: (2000, England) 40, 421.72 kg, yr, General Manufacturing Information: Benzoic acid, 5-amino-2-hydroxy-: ACTIVE, One of the top 25 English prescription pharmaceuticals in 2000.

Applications

Documented applications: Uses: Used to make dyes and light-sensitive paper, Also used as a gastrointestinal anti-inflammatory drug, [Merck Index] A metabolite of the drug sulfasalazine, [REPROTOX], In manufacture of light-sensitive paper, azo and sulfur dyes, Treatment of ulcerative colitis (England), It is used orally, in a delay-release formulation, as a retention enema, and as a suppository., THERAP CAT: Anti-inflammatory (gastrointestinal), Synthetic Polymer MALDI Matrix Compounds, Use (kg) in Switzerland (2009): >5000, Use (kg, approx.) in Germany (2009): >75000, exact) in Germany (2009): 96794, Use (kg) in USA (2002): 136000, Consumption (g per capita) in Switzerland (2009): 0.64, Consumption (g per capita, approx.) in Germany (2009): 0.92, exact) in Germany (2009): 1.2, Consumption (g per capita) in the USA (2002): 0.48, Excretion rate: 0.1, Calculated removal (%): 92.1, Use Classification: Pharmaceuticals, Methods of Manufacturing: Preparation by reduction of m-nitrobenzoic acid with Zn dust and HCl, Formulations, Preparations: ... The pharmaceutical industry has been developing different delivery systems for Multi-Matrix System (MMX) mesalamine for the treatment of Crohn's disease and ulcerative colitis. The new oral mesalamine formulation is a once-daily MMX tablet that delivers the mesalamine to the colon, making it most useful in the treatment of ulcerative colitis. The MMX coating matrix and coating system begin dissolution in the final portion of the ileum. ..., Oral: Capsules, extended-release: 250 mg Pentasa, (Shire), 500 mg Pentasa, (Shire). Tablets, delayed-release: 400 mg Asacol, (Procter & Gamble). Rectal: Suppositories: 500 mg Canasa, (Axcan Scandipharm), 1 g Canasa, (Axcan Scandipharm). Suspension: 4 g, 60 mL Mesalamine Suspension Enema, (Clay-Park), Mesalamine Suspension Enema, (Teva), Rowasa Suspension Enema (with potassium metabisulfite), (Solvay)., Oral: Tablet Delayed Release: 1.2 g Lialda (Shire)., Consumption Patterns: (2000, England) 40, 421.72 kg, yr, General Manufacturing Information: Benzoic acid, 5-amino-2-hydroxy-: ACTIVE, One of the top 25 English prescription pharmaceuticals in 2000..

Technical Profile

What this product is

Mesalamine is a chemical compound with CAS registry number 89-57-6 and molecular formula C7H7NO3 (molecular weight 153.14).

Identification

CAS number: 89-57-6

Its molecular formula C7H7NO3 comprises 7 C, 7 H, 1 N, 3 O atoms.

Also known as: Mesalamine · 美沙拉嗪 · 5-Aminosalicylic acid

Frequently Asked Questions

What is the CAS number of Mesalamine?

The CAS registry number of Mesalamine is 89-57-6.

What is the molecular formula and molecular weight of Mesalamine?

Molecular formula C7H7NO3, molecular weight 153.14.

What other names is Mesalamine known by?

It is also registered under: Mesalamine, 美沙拉嗪, 5-Aminosalicylic acid.

What are the documented applications of Mesalamine?

Recorded applications: Uses: Used to make dyes and light-sensitive paper, Also used as a gastrointestinal anti-inflammatory drug, [Merck Index] A metabolite of the drug sulfasalazine, [REPROTOX], In manufacture of light-sensitive paper, azo and sulfur dyes, Treatment of ulcerative colitis (England), It is used orally, in a delay-release formulation, as a retention enema, and as a suppository., THERAP CAT: Anti-inflammatory (gastrointestinal), Synthetic Polymer MALDI Matrix Compounds, Use (kg) in Switzerland (2009): >5000, Use (kg, approx.) in Germany (2009): >75000, exact) in Germany (2009): 96794, Use (kg) in USA (2002): 136000, Consumption (g per capita) in Switzerland (2009): 0.64, Consumption (g per capita, approx.) in Germany (2009): 0.92, exact) in Germany (2009): 1.2, Consumption (g per capita) in the USA (2002): 0.48, Excretion rate: 0.1, Calculated removal (%): 92.1, Use Classification: Pharmaceuticals, Methods of Manufacturing: Preparation by reduction of m-nitrobenzoic acid with Zn dust and HCl, Formulations, Preparations: ... The pharmaceutical industry has been developing different delivery systems for Multi-Matrix System (MMX) mesalamine for the treatment of Crohn's disease and ulcerative colitis. The new oral mesalamine formulation is a once-daily MMX tablet that delivers the mesalamine to the colon, making it most useful in the treatment of ulcerative colitis. The MMX coating matrix and coating system begin dissolution in the final portion of the ileum. ..., Oral: Capsules, extended-release: 250 mg Pentasa, (Shire), 500 mg Pentasa, (Shire). Tablets, delayed-release: 400 mg Asacol, (Procter & Gamble). Rectal: Suppositories: 500 mg Canasa, (Axcan Scandipharm), 1 g Canasa, (Axcan Scandipharm). Suspension: 4 g, 60 mL Mesalamine Suspension Enema, (Clay-Park), Mesalamine Suspension Enema, (Teva), Rowasa Suspension Enema (with potassium metabisulfite), (Solvay)., Oral: Tablet Delayed Release: 1.2 g Lialda (Shire)., Consumption Patterns: (2000, England) 40, 421.72 kg, yr, General Manufacturing Information: Benzoic acid, 5-amino-2-hydroxy-: ACTIVE, One of the top 25 English prescription pharmaceuticals in 2000..

PubChem Public Data

Independent reference data for Mesalamine (CAS 89-57-6), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number89-57-6
PubChem CID4075
Molecular formulaC7H7NO3
IUPAC name5-amino-2-hydroxybenzoic acid
UNII (FDA)4Q81I59GXC

Computed descriptors

Molecular Weight153.14
XLogP31.3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass153.042593085
Monoisotopic Mass153.042593085
Topological Polar Surface Area83.6
Heavy Atom Count11

Physicochemical values on record

Melting Point260-280 °C
Melting Point283 °C
Solubility0.84
Solubility1.22e+01 g/L
Vapor Pressure0.00000006 [mmHg]
LogP1.2
LogP0.48

Documented uses on record

    Used to make dyes and light-sensitive paper; Also used as a gastrointestinal anti-inflammatory drug; [Merck Index] A metabolite of the drug sulfasalazine; [REPROTOX]In manufacture of light-sensitive paper, azo and sulfur dyes

    Synonyms and trade names

    5-Aminosalicylic acid; mesalamine; 89-57-6; Mesalazine; 5-Amino-2-hydroxybenzoic acid; 5-ASA; Fisalamine; Lialda; m-Aminosalicylic acid; Benzoic acid, 5-amino-2-hydroxy-; Mesalazina; sfRowasa; Apriso; p-Aminosalicylsaeure; Asacolitin; Mesalazinum

    Regulatory listings held on file

    GHS notification summary0.5% (1 / 195)

    GHS hazard classification

    GHS notification summary0.5% (1 / 195)
    Reported hazard statementsH315 (81.5%), H317 (44.1%), H319 (81.5%), H335 (81%), H412 (17.9%)

    This chemical does not meet GHS hazard criteria for 0.5% (1 of 195) of reports.

    H315 (81.5%): Causes skin irritation [Warning Skin corrosion/irritation]

    What the public record says

    5-Aminosalicylic acid · CAS 89-57-6 · C7H7NO3. UNII 4Q81I59GXC. Melting Point: 260-280 °C; Melting Point: 283 °C; Solubility: 0.84.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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