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Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12-C 15, C 12-C 13 and C 10-C 13, for detergent use. [1] The C n H 2n+1 chain is unbranched. They are mainly produced as intermediate in the production of surfactants, for use in detergent. Since the 1960s, LABs have emerged as the dominant precursor of ...
Allyl alcohol is converted mainly to glycidol, which is a chemical intermediate in the synthesis of glycerol, glycidyl ethers, esters, and amines. Also, a variety of polymerizable esters are prepared from allyl alcohol, e.g. diallyl phthalate. [5] Allyl alcohol has herbicidal activity and can be used as a weed eradicant [9]) and fungicide. [8]
C12-C14 alcohol glycidyl ether (AGE) is an organic chemical in the glycidyl ether family. [2] It is a mixture of mainly 12 and 14 carbon chain alcohols, also called fatty alcohols that have been glycidated.
Within LAS itself the detergency of the various isomers are fairly similar, [13] [14] however their physical properties (Krafft point, foaming etc.) are noticeably different. [ 15 ] [ 16 ] In particular the Krafft point of the high 2-phenyl product (i.e. the least branched isomer) remains below 0 °C up to 25% LAS whereas the low 2-phenyl cloud ...
The synthesis of allyl glycidyl ether by condensation of allyl alcohol and epichlorohydrin. AGE can also be synthesized by monoepoxidation of diallyl ether. [6] [7] The synthesis of allyl glycidyl ether by epoxidation of diallyl ether. Diepoxidation of the second alkene would produce diglycidyl ether. Allyl glycidyl ether is chiral.
Erucyl alcohol (cis-13-docosen-1-ol) 22 carbon atoms: unsaturated: C 22 H 44 O Lignoceryl alcohol (1-tetracosanol) 24 carbon atoms: C 24 H 50 O Ceryl alcohol (1-hexacosanol) 26 carbon atoms: C 26 H 54 O 1-Heptacosanol: 27 carbon atoms: C 27 H 56 O Montanyl alcohol, cluytyl alcohol, or 1-octacosanol: 28 carbon atoms: C 28 H 58 O 1-Nonacosanol ...