Search results
Results From The WOW.Com Content Network
N1-Methylpseudouridine is the methylated derivative of pseudouridine.It is used in in vitro transcription and for the production of RNA vaccines. [3] [4] In vertebrates, it stimulates significantly less activation of the innate immune response compared to uridine, [5] while the translation is stronger.
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]
37375–12–5 Ag 3 PO 4: silver phosphate: 7784–09–0 Ag 3 SbS 3: silver thioantimonate: 15983–65–0 Al: aluminium: 7429–90–5 AlAs: aluminium arsenide: 22831–42–1 AlB 2: aluminium diboride: 12041–50–8 AlB 12: aluminium dodecaboride: 12041–54–2 AlBr 3: aluminium bromide: 7727–15–3 AlBr 3 •6H 2 O: aluminium bromide ...
Solvent Red 26, also known as Oil Red EGN or C.I. 26120, is a purplish red synthetic azo dye.It is soluble in oils and insoluble in water. Its main use is as a standard fuel dye in the US mandated by the US IRS to distinguish low-taxed or tax exempt heating oil from automotive diesel fuel, and by the EPA to mark fuels with higher sulfur content; it is however increasingly replaced with Solvent ...
Diethylamino hydroxybenzoyl hexyl benzoate is an organic compound used in sunscreens to absorb UVA radiation. It is marketed as Parsol DHHB by DSM and as Uvinul A Plus by BASF.
Triacetin was first prepared in 1854 by the French chemist Marcellin Berthelot. [12] Triacetin was prepared in the 19th century from glycerol and acetic acid. [13] Its synthesis from acetic anhydride and glycerol is simple and inexpensive. 3 (CH 3 CO) 2 O + 1 C 3 H 5 (OH) 3 → 1 C 3 H 5 (OCOCH 3) 3 + 3 CH 3 CO 2 H
The top seven suppliers worldwide together had an annual capacity in 2001 of 179 kilotonnes (395 million pounds). DCPD was discovered in 1885 as a C 10 H 12 hydrocarbon among the products of pyrolysis of phenol by Henry Roscoe , who didn't identify the structure (that was made during the following decade) but accurately assumed that it was a ...
HT-0712 appears to act as a PDE4 inhibitor, thereby increasing cAMP levels. When cAMP levels are increased in neurons, this may trigger the activation of cAMP response element-binding proteins ().