Description

3,5-Dinitrobenzyl alcohol (CAS No. 71022-43-0) is a high-purity nitroaromatic compound with the molecular formula C₇H₆N₂O₅. This fine chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive benzyl alcohol group and electron-withdrawing nitro substituents. With a purity of ≥98%, it is ideal for precise applications requiring consistent performance. The compound is supplied as a crystalline solid with excellent stability under recommended storage conditions (2-8°C, protected from light and moisture). Its unique structure makes it a valuable intermediate for derivatization, catalysis, and specialty polymer synthesis. Suitable for laboratory and industrial-scale use, this product undergoes rigorous QC testing to ensure compliance with industry standards.

Properties

• CAS Number: 71022-43-0
• Complexity: 211
• IUPAC Name: (3,5-dinitrophenyl)methanol
• InChI: InChI=1S/C7H6N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-3,10H,4H2
• InChI Key: GPHYIQCSMDYRGJ-UHFFFAOYSA-N
• Exact Mass: 198.02767130
• Molecular Formula: C7H6N2O5
• Molecular Weight: 198.13
• SMILES: C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])CO
• Topological: 112
• Monoisotopic Mass: 198.02767130
• Synonyms: 3,5-Dinitrobenzyl alcohol, 71022-43-0, 3,5-DinitrobenzeneMethanol, Benzenemethanol, 3,5-dinitro-, 111Z6Y5YNW, EINECS 275-131-1, DTXSID90221262, BENZYL ALCOHOL, 3,5-DINITRO-, DTXCID90143753, 275-131-1, (3,5-Dinitrophenyl)methanol, MFCD00007235, 3,5-dinitrobenzylalcohol, (3,5-Dinitro-phenyl)-methanol, Benzenemethanol,3,5-dinitro-, UNII-111Z6Y5YNW, SCHEMBL716259, (3,5-Dinitrophenyl)methanol #, SCHEMBL11494117, SCHEMBL16958141, 3,5-Dinitrobenzyl alcohol, 98%, AKOS015913194, AKOS016003059, AC-37263, AS-58468, SY026001, DB-022111, CS-0132325, D4144, NS00037141, EN300-7410225, InChI=1/C7H6N2O5/c10-4-5-1-6(8(11)12)3-7(2-5)9(13)14/h1-3,10H,4H

3,5-Dinitrobenzyl alcohol serves as a key intermediate in the synthesis of nitroaromatic derivatives for pharmaceuticals and agrochemicals. It is employed in cross-coupling reactions and as a precursor for explosives research due to its energetic properties. Researchers also utilize it in polymer chemistry to modify resin systems and enhance material properties. Its electron-deficient aromatic ring makes it valuable in catalytic studies and ligand design.

Safety and Hazards

GHS Hazard Statements

• H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (100%)
• Skin Irrit. 2 (100%)
• Eye Irrit. 2A (100%)
• STOT SE 3 (100%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.