270423

Nitromethane

suitable for HPLC, ≥96%

• Formule empirique (notation de Hill): CH₃NO₂
• Numéro CAS: 75-52-5
• Poids moléculaire : 61.04
• Numéro Beilstein : 1698205
• Numéro CE : 200-876-6
• Numéro MDL: MFCD00007400
• Code UNSPSC : 12190000
• ID de substance PubChem : 329752938
• Nomenclature NACRES : NA.21

Propriétés

• Densité de vapeur: 2.1 (vs air)
• Niveau de qualité: 100
• Pression de vapeur: 2.7 mmHg
• Pureté: ≥96%
• Forme: liquid
• Température d'inflammation spontanée: 784 °F
• Limite d'explosivité: 7.3 %, 33 °F
• Technique(s): HPLC: suitable
• Impuretés: <0.030% water
• Indice de réfraction: n20/D 1.382 (lit.)
• pH: 6.4 (20 °C, 0.01 g/L)
• Point d'ébullition: 101.2 °C (lit.)
• Pf: −29 °C (lit.)
• Densité: 1.127 g/mL at 25 °C (lit.)
• λ: H₂O reference
• Absorption UV: λ: 380 nm A_max: 1.00; λ: 386 nm A_max: 0.50; λ: 395 nm A_max: 0.20; λ: 400 nm A_max: 0.10; λ: 405 nm A_max: 0.05; λ: 430-700 nm A_max: 0.01
• Application(s): food and beverages
• Chaîne SMILES: C[N+]([O-])=O
• InChI: 1S/CH3NO2/c1-2(3)4/h1H3
• Clé InChI: LYGJENNIWJXYER-UHFFFAOYSA-N

Description

Application

• Asymmetric aza-Henry reaction toward trifluoromethyl β-nitroamines and biological investigation of their adamantane-type derivatives.: This study used nitromethane in asymmetric aza-Henry reactions to synthesize trifluoromethyl β-nitroamines, which were further investigated for their biological properties, showcasing the potential of nitromethane in advanced synthetic chemistry (Ren et al., 2024).


• Effect of Temperature on the Liquid Bridging Force while Maintaining Physical Stability in Solid-Liquid Mixed Fuel.: Nitromethane was analyzed in this research to understand its role in the stability of solid-liquid mixed fuels under varying temperatures, providing insights into the optimization of fuel formulations (Zhang et al., 2024).


• Generation of New Synthons for Synthesis Through Activation of Nitromethane.: This research demonstrated the activation of nitromethane to generate new synthons for synthetic applications, highlighting its versatility and importance in creating novel chemical entities (Wang et al., 2024).


• Towards Chemoenzymatic Syntheses of Both Enantiomers of Phosphoemeriamine.: The study explored the use of nitromethane in chemoenzymatic syntheses, enabling the production of both enantiomers of phosphoemeriamine, an important compound in chemical biology (Kiełbasiński et al., 2024).


• Rationally introducing non-canonical amino acids to enhance catalytic activity of LmrR for Henry reaction.: Nitromethane was employed in this study to investigate the enhancement of catalytic activity in the Henry reaction through the introduction of non-canonical amino acids, demonstrating its significance in enzyme catalysis research (Wang et al., 2024).

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Informations sur la sécurité

• Pictogrammes: GHS02,GHS08,GHS07
• Mention d'avertissement: Warning
• Mentions de danger: H226,H302 + H332,H351,H361d
• Conseils de prudence: P202 - P210 - P233 - P301 + P312 - P304 + P340 + P312 - P308 + P313
• Classification des risques: Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 3 - Repr. 2
• Code de la classe de stockage: 4.1A - Other explosive hazardous materials
• Classe de danger pour l'eau (WGK): WGK 2
• Point d'éclair (°F): 95.0 °F - closed cup
• Point d'éclair (°C): 35 °C - closed cup