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Propyl-methoxyphenol

When considering biomass as a source of chemical feedstock, it is also important to remember that it is not a homogeneous organic structure. The carbohydrate structures of terrestrial plants are composed of both five-carbon and six-carbon sugar polymers. The lignin component, which binds the polymers together, is an aromatic polymer of nominally propyl-methoxyphenols. In addition, there are proteins and fatty acids/oils, as well as the trace biocomponents that incorporate much of the mineral content. Therefore, processing biomass to chemical products must take into consideration both its bulk chemical structure and its components. [Pg.808]

Figure 6.11 Resulting chromatogram from a Simplex optimization procedure applied to the separation of three antioxidants. Solvents 5% acetonitrile in water (A) and 5% water in acetonitrile (B). Linear gradient 44 to 100% B in A in 1.5 min. Column 10 cm x 5 mm I.D. 5 pm Lichrosorb C-18. Flow rate 2.0 mL/min. Solutes 1 = propyl gallate 2 = 2-t-butyl-p-methoxyphenol (BHA) 3 = unknown 4 = 2,6-di-t-bytul-p-cresol (BHT). Figure taken from ref. [621J. Reprinted with permission. Figure 6.11 Resulting chromatogram from a Simplex optimization procedure applied to the separation of three antioxidants. Solvents 5% acetonitrile in water (A) and 5% water in acetonitrile (B). Linear gradient 44 to 100% B in A in 1.5 min. Column 10 cm x 5 mm I.D. 5 pm Lichrosorb C-18. Flow rate 2.0 mL/min. Solutes 1 = propyl gallate 2 = 2-t-butyl-p-methoxyphenol (BHA) 3 = unknown 4 = 2,6-di-t-bytul-p-cresol (BHT). Figure taken from ref. [621J. Reprinted with permission.
METHYL-l-PROPYL ACRYLATE (106-63-8) Forms explosive mixture with air (flash point 94°F/34°C). Will polymerize in elevated temperatures (recommended inhibitor 5 ppm hydroquinone or 10-60 ppm p-methoxyphenol). Uncontrolled bulk polymerization can be explosive. Incompatible with strong acids, ahphatic amines, alkanolamines. Flow or agitation of substance may generate electrostatic charges due to low conductivity. [Pg.802]

Synonyms Cerulignol Guaiacylpropane 1-(4-Hydroxy-3-methoxyphenyl) propane (4-Hydroxy-3-methoxyphenyl) propane 4-H y d roxy-3- m et h oxypro py I benzene 2-Methoxy-4-propylphenol 2-Methoxy-4-(1-propyl) phenol 2-Methoxy-4-n-propylphenol Phenol, 2-methoxy-4-propyl- 4-Propylguaiacol p-Propylguaiacol p-n-Propylguaiacol 4-Propylguaiacolcatechol 5-Propyl-o-hydroxyanisole 1-Propyl-3-methoxy-4-hydroxybenzene 4-Propyl-2-methoxyphenol... [Pg.1336]

Propyl methoxybenzene. See p-Propyl anisole 1 -Propyl-3-methoxy-4-hydroxybenzene 4-Propyl-2-methoxyphenol. See Dihydroeugenol Propyl-2-methyl butyrate CAS 37064-20-3 Properties Flash pt. (CC) 42 C Uses Fragrance flavor... [Pg.3761]

To determine antioxidants in food oils, Vigneron and Spicht [8] extracted an hexane solution of the oil with 1 % ammonium acetate, 32% aqueous acetonitrile and 48% aqueous acetonitrile to isolate propyl, octyl and dodecyl gallates, respectively. As traces of t-butyl-4-methoxyphenol were also extracted by the last solvent, a hexane solution of another portion of the sample was extracted with 30% water (to remove the gallates) and washed with aqueous ammonia, then the BHA was extracted with 72% aqueous ethanol and the BHT remains in the hexane solution. [Pg.299]


See other pages where Propyl-methoxyphenol is mentioned: [Pg.342]    [Pg.146]    [Pg.265]    [Pg.310]    [Pg.344]    [Pg.231]    [Pg.302]    [Pg.607]    [Pg.300]    [Pg.252]   
See also in sourсe #XX -- [ Pg.4 , Pg.10 ]




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