02487

Cloroformo

analytical standard

• Sinónimos: Triclorometano, Tricloruro de metilidino
• Fórmula empírica (notación de Hill): CHCl₃
• Número de CAS: 67-66-3
• Peso molecular: 119.38
• Beilstein: 1731042
• Número CE: 200-663-8
• Número MDL: MFCD00000826
• Código UNSPSC: 12191502
• ID de la sustancia en PubChem: 329747448
• NACRES: NA.24

Propiedades

• grado: analytical standard
• Nivel de calidad: 100
• densidad de vapor: 4.1 (vs air)
• presión de vapor: 160 mmHg ( 20 °C)
• Ensayo: ≥99.9% (GC)
• caducidad: limited shelf life, expiry date on the label
• contiene: ~0.003% amylene as stabilizer
• técnicas: HPLC: suitable; gas chromatography (GC): suitable
• índice de refracción: n20/D 1.444-1.447; n20/D 1.445 (lit.)
• bp: 60.5-61.5 °C (lit.)
• mp: −63 °C (lit.)
• densidad: 1.492 g/mL at 25 °C (lit.)
• aplicaciones: agriculture; cleaning products; cosmetics; environmental; food and beverages; personal care
• Formato: neat
• cadena SMILES: ClC(Cl)Cl
• InChI: 1S/CHCl3/c2-1(3)4/h1H
• Clave InChI: HEDRZPFGACZZDS-UHFFFAOYSA-N

Descripción

Descripción general

Chloroform is a colorless, volatile, liquid derivative of trichloromethane with an ether-like odor. It is a commonly used laboratory solvent. Presently, it is used in the industry as a solvent and in the production of the refrigerant freon. It is majorly used in production of chlorodifluoromethane, which is a refrigerant and fluoropolymer feedstock. It degrades in air to produce phosgene, dichloromethane, formyl chloride, CO, CO2 and hydrogen chloride. It can be orally consumed or inhaled, as it can be quickly absorbed, metabolized and eliminated by mammals.[1]

Aplicación

• Chloroform for organic synthesis: Chloroform is widely used in organic synthesis, providing a reliable solvent for the creation and purification of chemical compounds. It facilitates various reactions, including the integration of lipid analysis using advanced chromatographic techniques (Panczel et al., 2024).


• Chloroform as a catalyst in organic synthesis: Employed as a catalyst, chloroform enhances the catalytic efficiencies of various biochemical reactions, such as the activation methods in catalytic studies, aiding in the development of more efficient and sustainable chemical processes (Behera et al., 2024).

Productos recomendados

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Información de seguridad

• Pictogramas: GHS06,GHS08
• Palabra de señalización: Danger
• Frases de peligro: H302,H315,H319,H331,H336,H351,H361d,H372,H412
• Consejos de prudencia: P201 - P273 - P301 + P312 + P330 - P302 + P352 - P304 + P340 + P311 - P308 + P313
• Clasificaciones de peligro: Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3
• Órganos de actuación: Central nervous system, Liver,Kidney
• Código de clase de almacenamiento: 6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): does not flash
• Punto de inflamabilidad (°C): does not flash
• Equipo de protección personal: Eyeshields, Faceshields, Gloves