Description

3,5-Dinitrobenzohydrazide (CAS No. 2900-63-2) is a high-purity nitroaromatic compound with the molecular formula C₇H₆N₄O₅. This yellow crystalline powder is a versatile intermediate in organic synthesis, particularly for the preparation of heterocyclic compounds, hydrazone derivatives, and energetic materials. With a molecular weight of 226.15 g/mol, it exhibits excellent reactivity due to the presence of both nitro and hydrazide functional groups. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied in sealed containers to maintain stability. Ideal for researchers in pharmaceuticals, agrochemicals, and materials science seeking to exploit its electron-withdrawing and chelating properties.

Properties

• CAS Number: 2900-63-2
• Complexity: 287
• IUPAC Name: 3,5-dinitrobenzohydrazide
• InChI: InChI=1S/C7H6N4O5/c8-9-7(12)4-1-5(10(13)14)3-6(2-4)11(15)16/h1-3H,8H2,(H,9,12)
• InChI Key: IJVPILVRNBBRSO-UHFFFAOYSA-N
• Exact Mass: 226.03381930
• Molecular Formula: C7H6N4O5
• Molecular Weight: 226.15
• SMILES: C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])C(=O)NN
• Topological: 147
• Monoisotopic Mass: 226.03381930
• Synonyms: 3,5-Dinitrobenzohydrazide, 2900-63-2, 3,5-Dinitrobenzhydrazide, 3,5-dinitrobenzoylhydrazine, 3,5-dinitrobenzoyl hydrazide, 62DQ568XMD, EINECS 220-790-2, NSC-87798, Benzhydrazide, 3,5-dinitro-, DTXSID70183197, NSC 87798, 3,5-DINITROBENZOIC ACID HYDRAZIDE, 3,5-DINITROBENZENECARBOXYLIC ACID HYDRAZIDE, DTXCID80105688, 220-790-2, ijvpilvrnbbrso-uhfffaoysa-n, Benzoic acid, 3,5-dinitro-, hydrazide, 3,5-Dinitro-benzoic acid hydrazide, NSC87798, 3,5-Dinitrobenzhydrazid, NCIOpen2_005298, UNII-62DQ568XMD, 3,5-Dinitrobenzohydrazide #, benzohydrazide, 3,5-dinitro-, CHEMBL4089708, SCHEMBL10802488, 1,3-dinitrobenzene-5-carbohydrazide, MFCD00017060, STK364418, AKOS000116717, FD70500, SY133305, CS-0219366, NS00028599, ST50046194, EN300-03821, G54544, AE-641/02371051, Z56827597

Application

3,5-Dinitrobenzohydrazide serves as a key precursor in the synthesis of biologically active hydrazone derivatives for pharmaceutical research. Its nitro groups facilitate energetic material development, including propellants and explosives formulations. The compound is also employed in coordination chemistry as a ligand for transition metal complexes. Additionally, it finds use in analytical chemistry as a derivatization agent for carbonyl compound detection.

Safety and Hazards

GHS Hazard Statements

• H317 (97.4%): May cause an allergic skin reaction [Warning Sensitization, Skin]

Precautionary Statements

• P261, P272, P280, P302+P352, P321, P333+P317, P362+P364, and P501

Hazard Classes and Categories

• Skin Sens. 1 (97.4%)

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