Acrolein-DNPH solution - analytical standard, 100μg/ml in Acetonitrile , CAS No.888-54-0

CAS: 888-54-0 Cat. No.: A114137 Fórmula: C₉H₈N₄O₄ Peso molecular: 236.18 Número CE: 626-989-4

GRADE & PURITY Analytical standard, 100μg/ml in Acetonitrile

Synonyms

AS-40786 | Acrolein-2,4-dinitrophenylhydrazone, BCR(R) certified Reference Material | InChI=1/C9H8N4O4/c1-2-5-10-11-8-4-3-7(12(14)15)6-9(8)13(16)17/h2-6,11H,1H2/b10-5+ | Acrolein-2,4-dinitrophenylhydrazone 1000 microg/mL in Acetonitrile | Acrolein-2,4-DNP

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

AS-40786 | Acrolein-2,4-dinitrophenylhydrazone, BCR(R) certified Reference Material | InChI=1/C9H8N4O4/c1-2-5-10-11-8-4-3-7(12(14)15)6-9(8)13(16)17/h2-6,11H,1H2/b10-5+ | Acrolein-2,4-dinitrophenylhydrazone 1000 microg/mL in Acetonitrile | Acrolein-2,4-DNP

Especificações e pureza

analytical standard, 100μg/ml in Acetonitrile

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Grau

Padrão analítico

Nomes e identificadores

• Pubchem Sid: 508811697
• Sorrisos canónicos: C=CC=NNC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
• IUPAC Name: 2,4-dinitro-N-[(E)-prop-2-enylideneamino]aniline
• InChIKey: JJPZHGIYUVFTGG-BJMVGYQFSA-N
• INCHI: 1S/C9H8N4O4/c1-2-5-10-11-8-4-3-7(12(14)15)6-9(8)13(16)17/h2-6,11H,1H2/b10-5+
• SMILES isoméricas: C=C/C=N/NC1=C(C=C(C=C1)[N+](=O)[O-])[N+](=O)[O-]
• Peso molecular: 236.18
• Reaxy-Rn: 960602
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=960602&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Descrição: 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

Propriedades químicas e físicas

• Peso molecular: 236.180 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 236.055 Da
• Monoisotopic Mass: 236.055 Da
• Topological Polar Surface Area: 116.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 333.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

Referências

1. Mantong Zhao, Zhongyuan Liu, Mengyin Zha, Ying Sun, Haohao Shi, Xueying Zhang, Chuan Li, Guanghua Xia.  (2025)  Investigation of the dose and structure effects of lipid oxidation products aldehydes on the generation of heterocyclic amines: A case study of 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP).  Food Chemistry-X,      [PMID:39974535] [10.1016/j.fochx.2025.102244]

2. Hao Zhang, Shu Wang, Shixiao Wei, Shangde Sun, Yanlan Bi, Mingfu Wang, Yueliang Zhao.  (2025)  Development, validation and application of an SFC-ESI-QqQ-MS/MS method for simultaneous analysis of malondialdehyde and typical α,β-unsaturated aldehydes in edible oils and oil-containing foods.  FOOD CHEMISTRY,      [PMID:41332026] [10.1016/j.foodchem.2025.146795]

3. Zhang Hao, Chen Fenlin, Sun Shangde, Chen Xiaowei, Bi Yanlan, Qiu Shaohua, Yan Chao, Wang Mingfu, Zhao Yueliang.  (2026)  Mitigation of α,β-unsaturated Aldehydes in Fried Crisps and During In Vitro Digestion by Water-Insoluble Black Chokeberry Pomace: Insights into Phenolic Retention and Matrix-Bound Defenses.  Food and Bioprocess Technology,  19  (8): (424).  [PMID:] [10.1007/s11947-026-04515-7]