Formaldehyde 2,4-Dinitrophenylhydrazone - ≥98%(HPLC) , CAS No.1081-15-8

CAS: 1081-15-8 Cat. No.: F156631 Peso molecular: 210.15 Número EC: 628-494-9

GRADE & PURITY ≥98%(HPLC)

Synonyms

Formaldehyde-2,4-dinitrophenylhydrazone, analytical standard, for environmental analysis | Formaldehyde 2,4-Dinitrophenylhydrazone | UEQLSLWCHGLSML-UHFFFAOYSA-N | Methanal 2,4-dinitrophenylhydrazone | NSC 404128 | E78915 | SCHEMBL1666974 | Formaldehyde, (

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

Formaldehyde-2, 4-dinitrophenylhydrazone, analytical standard, for environmental analysis | Formaldehyde 2, 4-Dinitrophenylhydrazone | UEQLSLWCHGLSML-UHFFFAOYSA-N | Methanal 2, 4-dinitrophenylhydrazone | NSC 404128 | E78915 | SCHEMBL1666974 | Formaldehyde, (

Especificaciones y pureza

≥98%(HPLC)

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%(HPLC)

Nombres e identificadores

• Pubchem Sid: 504754552
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754552
• Sonrisas canónicas: C=NNC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
• IUPAC Name: N-(methylideneamino)-2,4-dinitroaniline
• InChIKey: UEQLSLWCHGLSML-UHFFFAOYSA-N
• INCHI: 1S/C7H6N4O4/c1-8-9-6-3-2-5(10(12)13)4-7(6)11(14)15/h2-4,9H,1H2
• Isómeros SMILES: C=NNC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
• Número ONU: UN1325
• Grupo de embalaje: III
• Peso molecular: 210.15
• Reaxy-Rn: 750330
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=750330&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: 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 Hydrazones Organopnictogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzene - Nitroaromatic compound - Phenylhydrazine - C-nitro compound - Organic nitro compound - Hydrazone - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic zwitterion - Organopnictogen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Punto de inflamación (°F): 2°C
• Punto de inflamación (°C): 2°C
• Punto de fusión (°C): 153-158°C
• Peso molecular: 210.150 g/mol
• XLogP3: 2.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 210.039 Da
• Monoisotopic Mass: 210.039 Da
• Topological Polar Surface Area: 116.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 271.000
• 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: 1

Referencias

1. Heng Zhao, Xiaolin Ma, Mingjie Lu, Fengting He, Feifei Lin, Yang Zhang, Jinqiang Zhang, Pei Dong, Chaocheng Zhao, Hongqi Sun.  (2022)  Melamine foam derived nitrogen and boron co-doped metal-free electrode for enhanced electro-Fenton degradation of metronidazole.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.140593]

2. Ping Chen, Xiaoyong Zhao, Hui Wang, Mengdan Zheng, Qinghua Wang, Wenjuan Chang.  (2022)  The Down-Regulation of lncRNA PCAT18 Promotes the Progression of Gastric Cancer via MiR-107/PTEN/PI3K/AKT Signaling Pathway.  OncoTargets and Therapy,      [PMID:31853187] [10.2147/OTT.S225235]

3. Yiwen Cao, Shenjie Zhu, Lin Zhang, Qun Cui, Haiyan Wang.  (2021)  Qualitative and quantitative determination of trace aldehydes and ketones in food preservative propionic acid for quality improvement.  Analytical Methods,  13  (26): (2989-2996).  [PMID:34124731] [10.1039/D1AY00742D]