Search results
Results From The WOW.Com Content Network
A standard method for the preparation of N-acylamino acids is the Schotten-Baumann reaction, in which oleoyl chloride (from oleic acid and, e.g. phosphorus trichloride) is added to an aqueous solution of N-methylglycine at pH 10 (kept constant by the addition of sodium hydroxide solution).
CAS number NBr 3: nitrogen tribromide: 15162–90–0 NCl 3: nitrogen trichloride: 10025–85–1 NF 3: nitrogen trifluoride: 7783–54–2 NH 3: ammonia: 7664–41–7 NH 4 Cl: ammonium chloride: 12125–02–9 NH 4 HCO 3: ammonium bicarbonate: 1066–33–7 NH 4 NO 3: ammonium nitrate: 6484–52–2 NH 4 OH: ammonium hydroxide: 1336–21–6 ...
Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate is significantly less volatile than simpler phenolic antioxidants such as butylhydroxytoluene (BHT). This makes it more suitable to stabilising plastics, as it is not driven out by the high temperatures experienced during plastic extrusion and moulding, [2] when they are heated to 150-320 °C (300–600 °F). [3]
The International Chemical Identifier (InChI, pronounced / ˈ ɪ n tʃ iː / IN-chee) [3] is a textual identifier for chemical substances, designed to provide a standard way to encode molecular information and to facilitate the search for such information in databases and on the web.
Methylethyl ketone oxime is the organic compound with the formula C 2 H 5 C(NOH)CH 3.This colourless liquid is the oxime derivative of methyl ethyl ketone. MEKO, as it is called in the paint industry, is used to suppress "skinning" of paints: the formation of a skin on paint before it is used.
Octyl methoxycinnamate or ethylhexyl methoxycinnamate or octinoxate (), trade names Eusolex 2292 and Uvinul MC80, is an organic compound that is an ingredient in some sunscreens and lip balms.
The mechanism begins by generation of Si(CH 3) 3 X and a highly reactive [CF 3] − (trifluoromethide) intermediate. The [CF 3 ] − attacks the carbonyl to generate an alkoxide anion. The alkoxide is silylated by the reagent to give the overall addition product, plus [CF 3 ] − , thus propagating an anionic chain reaction.
Isobornyl cyclohexanol (IBCH, Sandenol) is an organic compound used primarily as a fragrance because of its aroma which is similar to sandalwood oil.Its chemical structure is closely related to that of both α-santalol and β-santalol, [4] which are the primary constituents of sandalwood oil.