1,4-Dinitrobenzene - analytical standard, for environmental analysis, ≥99.9% , CAS No.100-25-4

CAS: 100-25-4 Cat. No.: D100641 Peso molecular: 168.11 Beilstein Registry Number: 1105828 Número EC: 202-833-7

GRADE & PURITY Analytical standard, for Environmental analysis, ≥99.9%

Synonyms

1,4-Dinitrobenzene|100-25-4|P-DINITROBENZENE|Benzene, 1,4-dinitro-|Benzene, p-dinitro-|Dithane A-4|Dinitrobenzene, p-|para-Dinitrobenzene|1,4-Dinitro-benzene|DTXSID0021836|CHEBI:51398|NSC-3809|784Q9O56S9|Dinitrobenzene, para-|1,4-Dinitrobenzene, analytica

Storage

Room temperature

Shipped In

FedEx DG Service

Specifications

Sinónimos

1, 4-Dinitrobenzene | 100-25-4 | P-DINITROBENZENE | Benzene, 1, 4-dinitro- | Benzene, p-dinitro- | Dithane A-4 | Dinitrobenzene, p- | para-Dinitrobenzene | 1, 4-Dinitro-benzene | DTXSID0021836 | CHEBI:51398 | NSC-3809 | 784Q9O56S9 | Dinitrobenzene, para- | 1, 4-Dinitrobenzene, analytica

Especificaciones y pureza

analytical standard, for environmental analysis, ≥99.9%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

FedEx DG Service

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Grado

Analytical standard, for Environmental analysis

Pureza

≥99.9%

Nombres e identificadores

• Pubchem Sid: 504751361
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751361
• Sonrisas canónicas: C1=CC(=CC=C1[N+](=O)[O-])[N+](=O)[O-]
• IUPAC Name: 1,4-dinitrobenzene
• InChIKey: FYFDQJRXFWGIBS-UHFFFAOYSA-N
• INCHI: 1S/C6H4N2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4H
• Isómeros SMILES: C1=CC(=CC=C1[N+](=O)[O-])[N+](=O)[O-]
• WGK Alemania: 3
• RTECS: CZ7525000
• Número ONU: 3443
• Grupo de embalaje: II
• Peso molecular: 168.11
• Beilstein: 1105828
• Reaxy-Rn: 1105828
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1105828&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: Nitroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzene - Nitroaromatic compound - Organic nitro compound - C-nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - 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: dinitrobenzene

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

Objetivos asociados (humanos)

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Salmonella typhimurium (15756 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Slightly soluble in water, soluble in ethanol, ether, benzene, etc.
• Punto de inflamación (°F): 150℃
• Punto de inflamación (°C): 150℃
• Punto de ebullición (°C): 299°C
• Punto de fusión (°C): 174°C
• Peso molecular: 168.110 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 168.017 Da
• Monoisotopic Mass: 168.017 Da
• Topological Polar Surface Area: 91.600 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 165.000
• 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. Deyi Zhan, Abdul Saeed, Zixuan Li, Chengming Wang, Zhiwu Yu, Junfeng Wang, Nanjing Zhao, Weihong Xu, Jinhuai Liu.  (2020)  Highly fluorescent scandium-tetracarboxylate frameworks: selective detection of nitro-aromatic compounds, sensing mechanism, and their application.  DALTON TRANSACTIONS,  49  (48): (17737-17744).  [PMID:33237063] [10.1039/D0DT03781H]

2. Tao Lu, Yuan Yuan, Yan Jiao, Zhining Wen, Lu Wang, Yihuan Zhao, Yuxiang Zhang, Menglong Li, Xuemei Pu, Tao Xu.  (2016)  Simultaneous spectrophotometric quantification of dinitrobenzene isomers in water samples using multivariate calibration methods.  CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS,      [PMID:] [10.1016/j.chemolab.2016.03.022]

3. Xiaoyu Liu, Wenhao Wu, Daohui Lin, Kun Yang.  (2024)  Linear adsorption of organic compounds on mesoporous activated carbon in bi-solute system.  Heliyon,      [PMID:38352802] [10.1016/j.heliyon.2024.e25729]

4. Chunyan Liu, Yanjuan Liu, Yuefei Zhang, Wei Chen, Sheng Tang.  (2024)  Synergistic expression of ZIF-67 and amphiphilic polymer hydrogel in multi-mode liquid chromatographic separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.127827]

5. Weijie Shang, Yanjie Huang, Yihang Zhang, Ruojia Li, Liping Dai.  (2025)  Quantification of Fatty Acids from Arctium lappa L. Leaves by 13C qNMR and HPLC-CAD.  Journal of Oleo Science,      [PMID:40887267] [10.5650/jos.ess25041]

6. Guoxi Deng, Yaotao Huang, Mingxian Liu, Xiaodan Chen, Yuri Lvov.  (2026)  Aqueous-phase synthesis of Ni2P within clay nanotube lumens for efficient catalytic nitroarene hydrogenation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41581452] [10.1016/j.jcis.2026.139948]