N-Hexadecanol

Heterocyclics 252, 260, 299,416 n-Hexadecanol esters 63 Hexaporphyrin 102 Hexitols 426 Hexobarbital 254,255 Hexoses 161,202 Hexuronic acid 158 Histamine 294,296, 355 Homogentisic acid 166,167 Horizontal chamber 127 Hotplates 93 ff -, temperature distribution 95 Hydrazines 269,284 Hydrazone formation 71 ff -with 2,4-dinitrophenylhydrazine 71, 72, 274... 

N-Heterocyclics la 252 lb 268 Hexachlorocyclohexane lb 227 Hexachlorocyclohexane isomers lb 211 Hexacyanoferrate(II) anions lb 307 Hexacyanoferrate(ni) anions lb 307 n-Hexadecanol esters, alkaline hydrolysis la 63... 

Abrahamsson S, Larsson G, von Sydow E. The crystal structure of n-hexadecanol. Acta Cryst 1960 13 770-774. 

Therapeutic Function Pharmaceutic aid Chemical Name n-Hexadecanol... 

HEXADECANOL see HCPOOO HEXADECAN-l-OL see HCPOOO n-HEXADECANOL see HCPOOO HEXADECENE EPOXIDE see EBX500... 

Figure 29 Vesicles made of the double-tailed surfactant (33) and containing in the internal water pool the quinolinium derivative (35) are destroyed by acetylcholinesterase, very probably leading to the formation of micelles made of (34) and n-hexadecanol. In the process, (35) is also released and cleaved by the enzyme [98]...

Tallow Alcohol. A name for commercial mixtures Of n-octadecano and n-hexadecanol. 

Beilstein Handbook Reference) Adol Adol 52 Adol 52 NF Adol 520 Adol 54 Adol 52 NF AI3-00755 Alcohol C-16 Aldol 54 Alfol 16 Atalco C BRN 1748475 C16 alcohol Cachalot C-50 Cachalot C-51 Cachalot C-52 Cachalo C-50 NF Caswell No. 165D Cetaffine Cetal Cetalol CA Cetanol 1-Cetanol Cetostearyl alcohol Cetyl alcohol n-Cetyl alcohol Cetylic alcohol Cetylol CO-1670 CO-1695 Crodacol C Crodacol-cas Crodacol-cat Cyclal cetyl alcohol Dytol F-11 EINECS 253-149-0 Elfacos C EPA Pesticide Chemical Code 001508 EPAL 16NF Ethal Ethol Fatty alcohol(C16) FEMA Number 2554 Hexadecanol n-Hexadecanol n-... 

The rate of evaporation of water decreases dramatically when a compact and coherent insoluble monolayer occupies the water-air interface (Gaines, 1966 La Mer, 1962). In this context, n-cetyl alcohol (n-hexadecanol) is a well-studied insoluble surfactant which forms such monolayers. A simple explanation is that a significant part of the interfacial area available for evaporation is blocked by the monolayer. Even at a liquid-liquid interface, a resistance to mass transfer is sometimes observed when a solute crosses the interface as it transfers from one liquid into another. This resistance appears to be independent of the convection in the liquid, suggesting that it lies solely at the interface (Chen and Lee, 2000). 

Berwanger R, Henschel A, Knorr K, Huber P, Pelster R (2009) Phase transitions nd molecular dynamics of n-hexadecanol confined in silicon nanochannels. Phys Rev B 79 125442 Buttard D, Bellet D, Dolino G (1996a) X-ray diflffaction investigation of the anodic oxidation of porous silicon. J Appl Phys 79 8060-8070... 

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