2,4-Dinitrophenylhydrazine hydrochloride - ≥98%(HPLC)(T),Used for high-performance liquid chromatography labeling , CAS No.55907-61-4

CAS: 55907-61-4 Cat. No.: D155225 Molecular Weight: 234.6 EC Number: 259-888-5

GRADE & PURITY ≥98%(HPLC)(T), Used for high-performance liquid chromatography labeling

Synonyms

Hydrazine, (2,4-dinitrophenyl)-, monohydrochloride | (2,4-dinitrophenyl)hydrazine hydrochloride | LS-13126 | SY060007 | 2,4-Dinitrophenyl hydrazine hydrochloride | 2,4-Dinitrophenylhydrazine hydrochloride | SCHEMBL1665136 | DTXSID40204505 | (2,4-dinitroph

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

Hydrazine, (2, 4-dinitrophenyl)-, monohydrochloride | (2, 4-dinitrophenyl)hydrazine hydrochloride | LS-13126 | SY060007 | 2, 4-Dinitrophenyl hydrazine hydrochloride | 2, 4-Dinitrophenylhydrazine hydrochloride | SCHEMBL1665136 | DTXSID40204505 | (2, 4-dinitroph

Specifications & Purity

≥98%(HPLC)(T), Used for high-performance liquid chromatography labeling

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%(HPLC)(T)

Names and Identifiers

• Canonical Smiles: C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NN.Cl
• IUPAC Name: (2,4-dinitrophenyl)hydrazine;hydrochloride
• InChIKey: PUYFAZQODQZOFK-UHFFFAOYSA-N
• INCHI: 1S/C6H6N4O4.ClH/c7-8-5-2-1-4(9(11)12)3-6(5)10(13)14;/h1-3,8H,7H2;1H
• Isomeric SMILES: C1=CC(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])NN.Cl
• Molecular Weight: 234.6
• Reaxy-Rn: 3636817
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3636817&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Nitrobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitrobenzenes
• Alternative Parents: Phenylhydrazines Nitroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic zwitterions Organic oxides Hydrochlorides Hydrocarbon derivatives Hydrazines and derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzene - Nitroaromatic compound - Phenylhydrazine - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Hydrazine derivative - Organic zwitterion - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organic salt - Hydrochloride - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
• 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

• Sensitivity: Air Sensitive,Hygroscopic
• Flash Point(°C): 80°C
• Molecular Weight: 234.600 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 234.016 Da
• Monoisotopic Mass: 234.016 Da
• Topological Polar Surface Area: 130.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 235.000
• 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: 2

XLogP3

References

1. Xi Peng, Xing Hu, Kai Liu, Deming Gong, Guowen Zhang.  (2023)  Exploring inhibitory effect and mechanism of hesperetin-Cu (II) complex against protein glycation.  FOOD CHEMISTRY,      [PMID:36870150] [10.1016/j.foodchem.2023.135801]

2. Lan Luo, Congcong Gu, Mingxian Li, Xiangyuan Zheng, Feng Zheng.  (2018)  Determination of residual 4-nitrobenzaldehyde in chloramphenicol and its pharmaceutical formulation by HPLC with UV/Vis detection after derivatization with 3-nitrophenylhydrazine.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:29730340] [10.1016/j.jpba.2018.04.024]