CHEBI:76394 - 2-nitro-p-phenylenediamine

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ChEBI Name 2-nitro-p-phenylenediamine ChEBI ID CHEBI:76394 ChEBI ASCII Name 2-nitro-p-phenylenediamine Definition A primary amino compound that is p-phenylenediamine in which one of the hydrogens attached to the benzene ring is replaced by a nitro group. It is a cosmetic hair dye intermediate that is used in permanent hair colouring products (diluted 1:1 with an oxidising agent prior to application). Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C6H7N3O2 Net Charge 0 Average Mass 153.13870 Monoisotopic Mass 153.05383 InChI InChI=1S/C6H7N3O2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H,7-8H2 InChIKey HVHNMNGARPCGGD-UHFFFAOYSA-N SMILES Nc1ccc(N)c(c1)[N+]([O-])=O Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) View more via ChEBI Ontology ChEBI Ontology Outgoing 2-nitro-p-phenylenediamine (CHEBI:76394) has functional parent 1,4-phenylenediamine (CHEBI:51403) 2-nitro-p-phenylenediamine (CHEBI:76394) is a C-nitro compound (CHEBI:35716) 2-nitro-p-phenylenediamine (CHEBI:76394) is a primary amino compound (CHEBI:50994) IUPAC Name 2-nitrobenzene-1,4-diamine Synonyms Sources 1,4-diamino-2-nitrobenzene ChemIDplus 1,4-Diaminonitrobenzol ChemIDplus 2,5-diaminonitrobenzene ChemIDplus 2-nitro-1,4-benzenediamine ChemIDplus 2-nitro-1,4-diaminobenzene ChemIDplus 2-nitro-1,4-phenylenediamine ChemIDplus 2-nitro-4-aminoaniline ChemIDplus 2-nitro-4-phenylenediamine ChemIDplus 2-NPPD NIST Chemistry WebBook 2NDB NIST Chemistry WebBook 4-amino-2-nitroaniline NIST Chemistry WebBook C.I. 76070 ChemIDplus CI 76070 ChemIDplus nitro-p-phenylenediamine NIST Chemistry WebBook o-nitro-p-phenylenediamine NIST Chemistry WebBook Manual Xref Database C19385 KEGG COMPOUND View more database links Registry Numbers Types Sources 2210195 Reaxys Registry Number Reaxys 5307-14-2 CAS Registry Number NIST Chemistry WebBook 5307-14-2 CAS Registry Number ChemIDplus Citations Types Sources 10873714 PubMed citation Europe PMC 12799694 PubMed citation Europe PMC 19469988 PubMed citation Europe PMC 2049801 PubMed citation Europe PMC 3594688 PubMed citation Europe PMC 520983 PubMed citation Europe PMC 6827626 PubMed citation Europe PMC 7327475 PubMed citation Europe PMC 7330774 PubMed citation Europe PMC 9465934 PubMed citation Europe PMC Last Modified 28 July 2014