| Identification | More | [Name]
2,2'-DINITROBIPHENYL | [CAS]
2436-96-6 | [Synonyms]
2,2'-DINITROBIPHENYL
2,2-DINITROBIPHENYL
2,2'-DINITRODIPHENYL
Dinitrobiphenyl
RARECHEM AQ BD 0003
2,2'-Dinitro-1,1'-biphenyl
2,2'-Dinitrobiphenyl, 2,2'-dinitro-
Biphenyl, 2,2'-dinitro-
1,1-Biphenyl, 2,2-dinitro-
2,2''-DINITROBIPHENYL 99+% | [EINECS(EC#)]
219-435-4 | [Molecular Formula]
C12H8N2O4 | [MDL Number]
MFCD00007127 | [Molecular Weight]
244.2 | [MOL File]
2436-96-6.mol |
| Chemical Properties | Back Directory | [Appearance]
light yellow to beige crystalline powder | [Melting point ]
124-126 °C(lit.) | [Boiling point ]
305°C | [density ]
1,45 g/cm3 | [refractive index ]
1.6360 (estimate) | [Fp ]
305°C | [storage temp. ]
Sealed in dry,2-8°C | [Water Solubility ]
Insoluble in water | [BRN ]
1579851 | [CAS DataBase Reference]
2436-96-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HS Code ]
29042090 |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow to beige crystalline powder | [Uses]
2,2′-Dinitrobiphenyl has been used as an internal standard in the determination of p,p′-DDT in technical and formulated products using gas chromatographic method. | [Uses]
2,2?-Dinitrobiphenyl has been used as an internal standard in the determination of p,p?-DDT in technical and formulated products using gas chromatographic method | [Definition]
ChEBI: Biphenyl substituted with nitro groups at the 2- and 2'-positions. | [Synthesis Reference(s)]
Organic Syntheses, Coll. Vol. 3, p. 339, 1955
The Journal of Organic Chemistry, 53, p. 4482, 1988 DOI: 10.1021/jo00254a012
Tetrahedron Letters, 16, p. 143, 1975 | [General Description]
The electroreduction of 2,2′-dinitrobiphenyl in anionic, cationic, and nonionic micellar solutions has been studied by polarography and cyclic voltammetry. | [Purification Methods]
Crystallise the biphenyl from EtOH, AcOH (m 124.5o) or pet ether (m 125.5-126o). [Beilstein 5 H 538, 5 III 1759, 5 IV 1826.] |
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