WebAcros Organics Dichloromethane, anhydrous, 99.9%, (1l) Zoom Image. Representative image only. Add to Compare. Acros Organics – Mfr # AC610300010 – Item # EW-88364-47. Consistent, high quality organics and fine chemicals at great savings. Reagents and solutions to meet your lab and research needs. MORE +. Web0.1 M DESC in anhydrous DMF: ... Dichloromethane, otherwise known as methylene chloride, is a common solvent in paint remover and is used for liquid–liquid extraction in laboratories. Acute toxicity is caused by CNS depression, and fatalities have resulted from exposure. Symptoms include mental confusion, fatigue, lethargy, headache, and ...
Dichloromethane, 99.9%, Extra Dry, anhydrous, SC, AcroSeal , …
WebOct 25, 2024 · The electrode was rinsed with anhydrous acetonitrile after electropolymerization and dried with nitrogen. The electrode was then soaked in 1.0 M BBr 3 in dichloromethane overnightat room temperature under ambient atmosphere for complete removal of the methyl groups. WebCauses serious eye irritation. May cause respiratory irritation. May cause drowsiness or dizziness. Suspected of causing cancer. May cause damage to organs through prolonged or repeated exposure. GHS P Statement Use personal protective equipment as required. Obtain special instructions before use. citizens icon holding
Dichloromethane CAS 75-09-2 DX0834 - EMD Millipore
WebThe resting cells were taken in phosphate buffer (0.05M; pH 7.0). Each substrate was added separately (2 mg/25 ml buffer) and incubated at 30°C for 6 h, after the reaction the flavouring compounds were extracted in dichloromethane, dried over anhydrous sodium sulphate, identified and analysed by GCMS. Dichloromethane (DCM or methylene chloride, methylene bichloride) is an organochlorine compound with the formula CH2Cl2. This colorless, volatile liquid with a chloroform-like, sweet odour is widely used as a solvent. Although it is not miscible with water, it is slightly polar, and miscible with many organic solvents. WebApr 9, 2024 · To a solution of tert-butyl ester 8 (1.66 g, 3.38 mmol) in anhydrous methylene chloride (28 mL), trifluoroacetic acid (11 mL) was added, and the mixture was stirred for 2 h at room temperature. The reaction progress was monitored by HPLC for the consumption of starting material. dickies carpenter short overalls