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Phenazopyridine hydrochloride | CAS:136-40-3
Phenazopyridine hydrochloride
  • Name:Phenazopyridine hydrochloride
  • CAS:136-40-3
  • Synonyms:2,6-Diamino-3-phenylazopyridine hydrochloride; Urodine
  • Molecular Formula:C11H11N5.HCl;C11H12ClN5
  • Molecular Weight:249.70
  • EINESC:205-243-8

Description

Properties

Melting point 139 ºC
Water Solubility 0.01-0.1 g/100 mL at 20 ºC

Safety

Symbol(GHS) Xn
Hazard Codes R22;R36/37/38;R40
SDS/MSDS S26;S36/37

SDS

Source SDS/MSDS Samples
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Synthetic Route
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Articles
Peer-Reviewed Papers
Oxidized cellulose--survey of the most recent achievements.Sergiu Coseri et al.Carbohydrate polymers, 93(1), 207-215 (2013-03-08) Pyrazolate-based cobalt(II)-containing metal-organic frameworks in heterogeneous catalytic oxidation reactions: elucidating the role of entatic states for biomimetic oxidation processes.Markus Tonigold et al.Chemistry (Weinheim an der Bergstrasse, Germany), 17(31), 8671-8695 (2011-06-21) Biomimetic catalytic system driven by electron transfer for selective oxygenation of hydrocarbon.Guanyu Yang et al.Journal of the American Chemical Society, 126(34), 10542-10543 (2004-08-26) Tetrahedron Letters, 33, 2645-2645 (1992) Unified QSAR approach to antimicrobials. 4. Multi-target QSAR modeling and comparative multi-distance study of the giant components of antiviral drug-drug complex networks.Francisco J Prado-Prado et al.Bioorganic & medicinal chemistry, 17(2), 569-575 (2008-12-30) Metal-free, NHPI catalyzed oxidative cleavage of C-C double bond using molecular oxygen as oxidant.Riyuan Lin et al.Organic letters, 14(16), 4158-4161 (2012-08-03) Radical amination of C(sp3)-H bonds using N-hydroxyphthalimide and dialkyl azodicarboxylate.Yuuki Amaoka et al.The Journal of organic chemistry, 77(22), 9959-9969 (2012-11-02) Bromide-free oxidizing system for carboxylic moiety formation in cellulose chain.Sergiu Coseri et al.Carbohydrate polymers, 90(4), 1415-1419 (2012-09-05) Application of a dual linker with a reference cleavage site to discover a new reaction between amines and N-hydroxyphthalimide.Viktor Krchnák et al.Journal of combinatorial chemistry, 7(4), 523-525 (2005-07-12) Oxidation of phenols by laccase and laccase-mediator systems.Francesca D'Acunzo et al.European journal of biochemistry, 269(21), 5330-5335 (2002-10-24) The copper-mediated cross-coupling of phenylboronic acids and N-hydroxyphthalimide at room temperature: synthesis of aryloxyamines.H M Petrassi et al.Organic letters, 3(1), 139-142 (2001-06-30) A kinetic study of the electron-transfer reaction of the phthalimide-N-oxyl radical (PINO) with ferrocenes.Enrico Baciocchi et al.The Journal of organic chemistry, 72(23), 8748-8754 (2007-10-24) [Contact allergy to dicyclohexylcarbodiimide and N-hydroxyphthalimide].M H Lang et al.Dermatosen in Beruf und Umwelt. Occupation and environment, 35(6), 212-213 (1987-11-01) Contact allergy to N-hydroxyphthalimide.S Fregert et al.Contact dermatitis, 9(1), 84-85 (1983-01-01) Controlling mode selectivity in palladium-catalyzed bisdiene carbocyclizations: optimizing for cyclization-trapping over cycloisomerization.James M Takacs et al.Organic letters, 5(20), 3595-3598 (2003-09-26) Crystal growth and characterization of N-hydroxyphthalimide (C8H5NO3) crystal.V Krishnakumar et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 110-115 (2008-01-26) Anthrone-derived NHPI analogues as catalysts in reactions using oxygen as an oxidant.Juan Shen et al.Organic & biomolecular chemistry, 6(22), 4096-4098 (2008-10-31) Mild and selective oxidation of cellulose fibers in the presence of N-hydroxyphthalimide.S Coseri et al.Biomacromolecules, 10(8), 2294-2299 (2009-09-03) [Hydroxyphthalimide induced medicamentosa-like dermatitis in five patients].Jian-fang Zou et al.Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 24(10), 625-625 (2006-11-14) Fluorous tagged N-hydroxy phthalimide for the parallel synthesis of O-aryloxyamines.Florence S Gaucher-Wieczorek et al.Journal of combinatorial chemistry, 12(5), 655-658 (2010-09-14)
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