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Phenazopyridine hydrochloride

HCID 8691
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
136-40-3
Standard SMILES
Cl.Nc1ccc(N=Nc2ccccc2)c(N)n1
InChIKey
QQBPIHBUCMDKFG-UHFFFAOYSA-N
Molecular formula
C11H12ClN5
Average molar mass
249.7 g/mol
Monoisotopic mass
249.0781231

Overview

Phenazopyridine Hydrochloride can cause cancer according to an independent committee of scientific and health experts.

Names & identifiers

Preferred name
Phenazopyridine hydrochloride
IUPAC
3-phenyldiazenylpyridine-2,6-diamine;hydrochloride
English name
Phenazopyridine hydrochloride
Molecular formula
C11H12ClN5
Molecular weight
249.7

Names & synonyms

Phenazopyridine hydrochloride136-40-3Phenazopyridine HClPyridiumUrodineMallophenePyripyridiumAzomineBisterilDiridoneSeduralSuladyne
Show more names
nc150pyrizinuraziumuriplexdolonil
3-Phenylazo-2,6-diaminopyridine hydrochloridePhenazodinePyrazodineAzodynePiridPhenylazo tabletsDi-AzoPhenazopyridine.HCl

Database identifiers

CAS
136-40-3
PubChem CID
8691
DTXSID
DTXSID1021118
ChEMBL
CHEMBL1606101
ChEBI
CHEBI:71419
UNII
0EWG668W17

Properties

Computed structural properties

Topological polar surface area
89.7 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
5
Rotatable bonds
2
Heavy atoms
17
Formal charge
0
Complexity
237

Experimental & physicochemical properties

Solubility30.4 [ug/mL] (The mean of the results at pH 7.4)
Collision Cross Section147.8 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

Physicochemical properties

Melting point
238 °C · 238 °C
Boiling point
394.6 °C · 394.6°C (rough estimate)
Density
1.2645 · 1.2645 (rough estimate)
refractive index
1.611 · 1.6110 (estimate)
Flash point
Not applicable
storage temp.
2 · Sealed in dry,2-8°C
solubility
DMSO (Slightly, Heated), Methanol (Slightly, Heated)
pka
5.2 · 5.20
form
powder to crystal
color
Orange to Brown to Dark purple
Water Solubility
0.01 · 0.01-0.1 g/100 mL at 20 ºC

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Safety data

PPE
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
wgk
3
rtecs
US7875000
ridadr
2811
hs_code
29333990
Toxicity
LD50 orally in rats: 403 mg/kg (Becker, Swift)
risk_code
22-36/37/38-40-34-42/43
Signal word
Warning
Symbol(GHS)
GHS07,GHS08
hazard_code
Xn,C
safety_code
26-36/37-45-36/37/39-27-22
Storage Class
10 - Combustible liquids
target organs
Respiratory system
Hazard statements
H302-H315-H319-H335-H351
Hazard Classifications
Acute Tox. 4 OralCarc. 2Eye Irrit. 2Skin Irrit. 2STOT SE 3
Precautionary statements
P202-P261-P301+P312-P302+P352-P305+P351+P338-P308+P313

Chemistry & industry

Applications · 6 items

DescriptionPhenazopyridine 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.

UsesPhenazopyridine 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.

UsesAn azo dye used in treatment of urinary tract infections. Used as an analgesic (urinary tract).

Usesanticonvulsant, antieleptic

Usestherapeutic for urinary tract infections

General DescriptionBrick-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.

Upstream & downstream products

Upstream raw materials

phenyldiazene2,6-DiaminopyridineAniline
Additional notes · 1 item

DefinitionChEBI: 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.

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Related reactions

2 records
New reaction record
HRID 397020 reaction equation
HRID 397020As reactantuspto-grants-2003_08
HRID 2063231 reaction equation
HRID 2063231As reactantuspto-grants-2012_10

Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Merck
14 · 14,7210
Stability
Light Sensitive
Major Application
forensics and toxicologypharmaceutical (small molecule)
InChI
1S/C11H11N5.ClH/c12-10-7-6-9(11(13)14-10)16-15-8-4-2-1-3-5-8;/h1-7H,(H4,12,13,14);1H/b16-15+;
InChIKey
QQBPIHBUCMDKFG-GEEYTBSJSA-N
SMILES
Cl[H].Nc1ccc(\N=N\c2ccccc2)c(N)n1
Toxicology and Carcinogenesis
Bioassay of Phenazopyridine Hydrochloride for Possible Carcinogenicity (CASRN 136-40-3)
CAS DataBase Reference
136 · 136-40-3(CAS DataBase Reference)
FDA UNII
0 EWG668W17 · 0EWG668W17
Proposition 65 List
Phenazopyridine Hydrochloride
IARC
2 B · 2B (Vol. 24, Sup 7) 1987
EPA Substance Registry System
Phenazopyridine hydrochloride (136-40-3)
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
7 · GHS07,GHS08
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H335-H351
Precautionary statements
202 · P202-P261-P301+P312-P302+P352-P305+P351+P338-P308+P313
target organs
Respiratory system
PPE
95 · dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Codes
Xn,C
Risk Statements
22 · 22-36/37/38-40-34-42/43
Safety Statements
26 · 26-36/37-45-36/37/39-27-22
RIDADR
2811 · 2811
WGK Germany
3 · 3
RTECS
7875000 · US7875000
HS Code
29333990 · 29333990
Storage Class
10 · 10 - Combustible liquids
Hazard Classifications
4 OralCarc · Acute Tox. 4 OralCarc. 2Eye Irrit. 2Skin Irrit. 2STOT SE 3
Toxicity
50 orally · LD50 orally in rats: 403 mg/kg (Becker, Swift)