o-Phenylenediamine dihydrochloride - AR, ≥99% , CAS No.615-28-1

CAS: 615-28-1 Cat. No.: P100830 Molecular Weight: 181.06 Beilstein Registry Number: 3912045 EC Number: 210-418-7

GRADE & PURITY AR, ≥99%

Synonyms

1,2-BENZENEDIAMINE DIHYDROCHLORIDE [HSDB] | benzene-1,2-diamine dihydrochloride | DTXCID501140 | 1,2-Diaminobenzene Dihydrochloride | benzene-1,2-diamine;dihydrochloride | O-PHENYLENEDIAMINE 2HCL | 1,2-phenylenediamine bishydrochloride | Q26841263 | 1,2-P

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads,FedEx DG Service

Specifications

Synonyms

1, 2-BENZENEDIAMINE DIHYDROCHLORIDE [HSDB] | benzene-1, 2-diamine dihydrochloride | DTXCID501140 | 1, 2-Diaminobenzene Dihydrochloride | benzene-1, 2-diamine;dihydrochloride | O-PHENYLENEDIAMINE 2HCL | 1, 2-phenylenediamine bishydrochloride | Q26841263 | 1, 2-P

Specifications & Purity

AR, ≥99%

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads, FedEx DG Service

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

AR

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 504752233
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752233
• Canonical Smiles: C1=CC=C(C(=C1)N)N.Cl.Cl
• IUPAC Name: benzene-1,2-diamine;dihydrochloride
• InChIKey: RIIWUGSYXOBDMC-UHFFFAOYSA-N
• INCHI: 1S/C6H8N2.2ClH/c7-5-3-1-2-4-6(5)8;;/h1-4H,7-8H2;2*1H
• Isomeric SMILES: C1=CC=C(C(=C1)N)N.Cl.Cl
• WGK Germany: 3
• RTECS: ST0175000
• UN Number: 2811
• Packing Group: I
• Molecular Weight: 181.06
• Beilstein: 3912045
• Reaxy-Rn: 3912045

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Aniline and substituted anilines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Aniline and substituted anilines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aniline and substituted anilines
• Alternative Parents: Primary amines Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Solubility in water: Completely soluble; Slightly soluble in Ethanol; Insoluble in Ether
• Sensitivity: Light sensitive.
• Melt Point(°C): 205°C(dec.)(lit.)
• Molecular Weight: 181.060 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 180.022 Da
• Monoisotopic Mass: 180.022 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 62.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

References

1. Linglin Fu, Yifan Qian, Jinru Zhou, Huan Li, Yanbo Wang.  (2019)  Quantification of shellfish Arginine kinases by double-enhanced immunoassay employing magnetic beads and gold nanoparticles as carrier.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2019.108916]

2. Lu Sun, Qian-Yue Xu, Hai-Bo Wang.  (2025)  A magnetic separated-type ultrasensitive fluorescent DNA biosensor based on hydrogen peroxide triggered chemically driven redox-cycling system.  NEW JOURNAL OF CHEMISTRY,      [PMID:] [10.1039/D5NJ02324F]