Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

11-Hexadecenal

Chemical degradation of chlorophyll gives a number of substances including phytol The constitution of phytol is given by the name 3 7 11 15 tetramethyl 2 hexadecen 1 ol How many stereoisomers have this constitution" ... [Pg.322]

Shimizu S, S Jareonkitmongol, H Kawashima, K Akimoto, H Yamada (1991) Production of a novel wl-eicosa-pentaenoic acid by Mortierella alpina lS-4 grown on 1-hexadecene. Arch Microbiol 156 163-166. [Pg.88]

Ethylhexanol can be epoxidized with 1-hexadecene epoxide. This additive also helps reduce or prevent foaming. By eliminating the need for traditional oil-based components, the composition is nontoxic to marine life, biodegradable, environmentally acceptable, and capable of being disposed of at the drill site without costly disposal procedures [44]. [Pg.14]

Another recent patent (22) and related patent application (31) cover incorporation and use of many active metals into Si-TUD-1. Some active materials were incorporated simultaneously (e.g., NiW, NiMo, and Ga/Zn/Sn). The various catalysts have been used for many organic reactions [TUD-1 variants are shown in brackets] Alkylation of naphthalene with 1-hexadecene [Al-Si] Friedel-Crafts benzylation of benzene [Fe-Si, Ga-Si, Sn-Si and Ti-Si, see apphcation 2 above] oligomerization of 1-decene [Al-Si] selective oxidation of ethylbenzene to acetophenone [Cr-Si, Mo-Si] and selective oxidation of cyclohexanol to cyclohexanone [Mo-Si], A dehydrogenation process (32) has been described using an immobilized pincer catalyst on a TUD-1 substrate. Previously these catalysts were homogeneous, which often caused problems in separation and recycle. Several other reactions were described, including acylation, hydrogenation, and ammoxidation. [Pg.377]

Another very common phytochemical isolated was phytol (3,7,11, 15-tetramethyl-2-hexadecen-l-ol), the diterpenoid alcohol which forms the "tail" of chlorophyll. This compound is nearly insoluble in water, but when applied as a 0.1 mM (0.003 wt. %) solution in 0.1% DMS0 it increased onion germination while decreasing germination in sorghum, wheat, and carrot. The germination effects are significant at only the 95% level, but pretreatment studies are planned as part of other terpene chemistry studies at SRRC and LSI). [Pg.293]

CTAB = cetyltrimethylammonium bromide DDAB = didodecyldimethylammonium bromide DEG = diethylene glycol DOE = dioctyl ether DPE = diphenyl ether DS = dodecyl sulfate EG — ethylene glycol EtOH = ethanol HAD = hexadecylamine HD = 1-hexadecene OD = 1-octadecene HDD = 1,2-hexadecanediol ... [Pg.66]

A unique enyne pheromone component, Z13-hexadecen-ll-ynyl acetate, found in Thaumetopoea pityocampa was found to be produced by the sequential action of a A13 desaturase and a All acetylenase to form ynell-16 acid [43]. The dienyl intermediate Z13,ynell-16 acid was formed by the action of... [Pg.107]

FIGURE 9.24 Molar radioactivity of the reaction products when co-feeding n-hexa-decene-(l)-(l-14C) together with the synthesis gas to FT synthesis on cobalt. Catalyst 100Co-18Th02-100Kieselguhr (by weight), precipitated, 190°C, 1 bar, H2/CO = 2, Xc0 = 70%, 0.1 vol% of hexadecene-14C in the synthesis gas. [Pg.180]


See other pages where 11-Hexadecenal is mentioned: [Pg.313]    [Pg.242]    [Pg.407]    [Pg.559]    [Pg.597]    [Pg.681]    [Pg.474]    [Pg.474]    [Pg.474]    [Pg.474]    [Pg.785]    [Pg.441]    [Pg.305]    [Pg.305]    [Pg.305]    [Pg.301]    [Pg.301]    [Pg.427]    [Pg.435]    [Pg.436]    [Pg.113]    [Pg.372]    [Pg.384]    [Pg.921]    [Pg.667]    [Pg.459]    [Pg.904]    [Pg.52]    [Pg.305]    [Pg.921]    [Pg.242]    [Pg.287]    [Pg.288]    [Pg.289]    [Pg.956]    [Pg.123]    [Pg.60]    [Pg.48]    [Pg.315]    [Pg.179]   
See also in sourсe #XX -- [ Pg.138 , Pg.296 , Pg.318 ]

See also in sourсe #XX -- [ Pg.87 , Pg.88 , Pg.140 ]




SEARCH



1-Hexadecene

1-Hexadecene

1-Hexadecene epoxidation

1-Hexadecene epoxide

1-Hexadecene oxidation, products

14-Methyl-8-hexadecen

14-Methyl-8-hexadecenal

3.7.11.15- Tetramethyl-2-hexadecen-1 -ol,

3.7.11.15- Tetramethyl-2-hexadecenal

9-Hexadecen-16-olide

Hexadecen-16-olide (ambrettolide)

I- Hexadecene

Z-7-Hexadecenal

Z-ll-Hexadecenal

© 2024 chempedia.info