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Phenazopyridine hydrochloride

Phenazopyridine hydrochloride  Structure
CAS No.
136-40-3
Chemical Name:
Phenazopyridine hydrochloride
Synonyms
nc150;pirid;sedural;pyrizin;urazium;uriplex;URODINE;azodyne;dolonil;giracid
CBNumber:
CB0415453
Molecular Formula:
C11H12ClN5
Molecular Weight:
249.7
MOL File:
136-40-3.mol
Modify Date:
2024/5/28 19:59:05

Phenazopyridine hydrochloride Properties

Melting point 139°C
Boiling point 394.6°C (rough estimate)
Density 1.2645 (rough estimate)
refractive index 1.6110 (estimate)
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly, Heated), Methanol (Slightly, Heated)
form Liquid
color Clear to hazy colorless to yellow
Water Solubility 0.01-0.1 g/100 mL at 20 ºC
Merck 14,7210
Stability Light Sensitive
InChIKey QQBPIHBUCMDKFG-GEEYTBSJSA-N
CAS DataBase Reference 136-40-3(CAS DataBase Reference)
IARC 2B (Vol. 24, Sup 7) 1987
EPA Substance Registry System Phenazopyridine hydrochloride (136-40-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H315-H319-H335-H351
Precautionary statements  P202-P261-P301+P312-P302+P352-P305+P351+P338-P308+P313
Hazard Codes  Xn,C
Risk Statements  22-36/37/38-40-34-42/43
Safety Statements  26-36/37-45-36/37/39-27-22
RIDADR  2811
WGK Germany  3
RTECS  US7875000
HS Code  29333990
Toxicity LD50 orally in rats: 403 mg/kg (Becker, Swift)
NFPA 704
1
2 1

Phenazopyridine hydrochloride price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 34076 Phenazopyridine hydrochloride VETRANAL?, analytical standard 136-40-3 100MG ₹10662.63 2022-06-14 Buy
TCI Chemicals (India) B0022 3-Phenylazo-2,6-diaminopyridine Monohydrochloride 136-40-3 25G ₹6800 2022-05-26 Buy
Product number Packaging Price Buy
34076 100MG ₹10662.63 Buy
B0022 25G ₹6800 Buy

Phenazopyridine hydrochloride Chemical Properties,Uses,Production

Description

Phenazopyridine is an azo dye with analgesic properties. It decreases the bladder distension-induced firing rate of afferent bladder Aγ-fibers, but not C-fibers, in anesthetized rats when administered at a doses of 0.3, 1, and 3 mg/kg. Formulations containing phenazopyridine have been used as analgesics in the treatment of urinary tract infections.

Chemical Properties

Brick-Red Crystals

Uses

Phenazopyridine hydrochloride has been used for 50 years as an analgesic drug either alone or in combination with other drugs to reduce pain associated with urinary tract infection. An azo dye used in urinary tract infections. Also used as a local anesthetic. Exposure to phenazopyridine hydrochloride occurs during manufacture and formulation.

Definition

ChEBI: A hydrochloride obtained by combining phenazopyridine with one equivalent of hydrochloric acid. A local anesthetic that has topical analgesic effect on mucosa lining of the urinary tract. Its use is limited by problems with toxicity (primarily blood disord rs) and potential carcinogenicity.

General Description

Brick-red microcrystals with a slight violet luster or a purple powder. Aqueous solutions are yellow to brick-red and slightly acidic; they may be stabilized by the addition of 10% glucose. Slightly bitter taste.

Air & Water Reactions

Dust can be explosive when suspended in air at specific concentrations. Phenazopyridine hydrochloride may be sensitive to air and light. . Very slightly water soluble.

Reactivity Profile

Phenazopyridine hydrochloride is an azo compound. Azo, diazo, azido compounds can detonate. This applies in particular to organic azides that have been sensitized by the addition of metal salts or strong acids. Toxic gases are formed by mixing materials of this class with acids, aldehydes, amides, carbamates, cyanides, inorganic fluorides, halogenated organics, isocyanates, ketones, metals, nitrides, peroxides, phenols, epoxides, acyl halides, and strong oxidizing or reducing agents. Flammable gases are formed by mixing materials in this group with alkali metals. Explosive combination can occur with strong oxidizing agents, metal salts, peroxides, and sulfides.

Fire Hazard

Flash point data for Phenazopyridine hydrochloride are not available. Phenazopyridine hydrochloride is probably combustible.

Clinical Use

Phenazopyridine hydrochloride, 2,6-diamino-3-(phenylazopyridinehydrochloride (Pyridium), is a brick-red, finecrystalline powder. It is slightly soluble in alcohol, in chloroform,and in water.Phenazopyridine hydrochloride was formerly used asa urinary antiseptic. Although it is active in vitro againststaphylococci, streptococci, gonococci, and E. coli, it has nouseful antibacterial activity in the urine. Thus, its presentutility lies in its local analgesic effect on the mucosa of theurinary tract.
Usually, phenazopyridine is given in combination withurinary antiseptics. For example, it is available as Azo-Gantrisin, a fixed-dose combination with the sulfonamide antibacterialsulfisoxazole, and as Urobiotic, a combination withthe antibiotic oxytetracycline and the sulfonamide sulfamethizole. The drug is rapidly excreted in the urine, towhich it gives an orange-red color. Stains in fabrics may beremoved by soaking in a 0.25% solution of sodium dithionite.

Safety Profile

Confirmed carcinogen with experimental carcinogenic and tumorigenic data. A poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion. Human systemic effects by ingestion: somnolence, cyanosis, dlarrhea, nausea or vomiting, anuria or decreased urine volume, normocytic anemia, methemoglobinemiacarboxyhemoglobinemia, dehydration, changes in blood sodium levels. Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and HCl

Carcinogenicity

Phenazopyridine hydrochloride is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity fromstudies in experimental animals.

Phenazopyridine hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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2,6-diamino-3-(phenylazo)-pyridinmonohydrochloride pyrizin sedural thiosulfil-aforte urazium uridinal uriplex urobiotic-250 3-[(E)-phenyldiazenyl]pyridine-2,6-diamine hydrochloride BISTERIL 3-phenylazopyridine-2,6-diamine hydrochloride component of Azo-Mandelamine component of Azotrex component of Dolonil Phenazopyridine M hydrochloride WLN: T6NJ BZ CNUNR & FZ & GH MALLOPHENE 3-PHENYLAZO-2,6-DIAMINOPYRIDINE HYDROCHLORIDE 3-PHENYLAZO-2,6-DIAMINOPYRIDINE MONOHYDROCHLORIDE 3-(PHENYLAZO)-2,6-PYRIDINEDIAMINE, MONOHYDROCHLORIDE 3-BENZENEAZO-2,6-DIAMINOPYRIDINE MONOHYDROCHLORIDE 2,6-DIAMINO-3-[PHENYLAZO]PYRIDINE HYDROCHLORIDE 2,6-DIAMINO-3-(PHENYLAZO)PYRIDINE MONOHYDROCHLORIDE PHENYLAZODIAMINOPYRIDINE HYDROCHLORIDE PHENAZODINE PHENAZOPYRIDINE HCL PHENAZOPYRIDINE HYDROCHLORIDE PYRIDACIL PYRIDIATE PYRIDIUM URODINE 3-(phenylazo)-2,6-pyridinediamine,hydrochloride 6-pyridinediamine,3-(phenylazo)-monohydrochloride azodyne beta-phenylazo-alpha,alpha’-diaminopyridinehydrochloride diridone dolonil eucistin giracid mallofeen nc150 nci-c01672 nefrecil phenazopyridiniumchloride phenylazo-alpha,alpha’-diaminopyridinemonohydrochloride phenylazopyridinehydrochloride phenylazotablets phenyl-idium phenyl-idium200 pirid pyridivite pyripyridium 3-PHENYLAZO-2,6-DIAMINOPYRIDINE HYDROCHLORIDE 98+% 3-Phenylazo-2,6-diaminopyridineHCl 3-(Phenylazo)-2,6-pyridinediamine, Monohydrochloride, Pyridium, Pyridiate, Pyridacil, Mallophene, PHENAZOPYRIDINEHYDROCHLORIDE,USP 3-PHENYLAZO-2,6-DIAMINOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE HYDROCHLORIDE) 2,6-Diamino-3-(phenylazo)pyridine hydrochloride, Urodine