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Triethylamine is prepared by the alkylation of ammonia with ethanol: [10]. NH 3 + 3 C 2 H 5 OH → N(C 2 H 5) 3 + 3 H 2 O. The pK a of protonated triethylamine is 10.75, [4] and it can be used to prepare buffer solutions at that pH.
CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA) 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0 C 20 H 25 N 30: Lysergic acid diethylamide (LSD) 50–37–3 C 123 H 193 N 35 O 37: Common serum albumin (macromolecule) 9048–49–1 Ca(AlH 4) 2: calcium ...
C 8 F 14 O 3: heptafluorobutyric anhydride: 336-59-4 C 8 F 16: perfluoroethylcyclohexane: 335-21-7 C 8 F 17 I: perfluorooctyl iodide: 507-63-1 C 8 F 18: perfluorooctane: 307-34-6 C 8 H(NO 2) 7: heptanitrocubane: 99393-62-1 C 8 H 2 Cl 4 O 2: fthalide: 27355-22-2 C 8 H 2 F 4 O 4: tetrafluorophthalic acid: 652-03-9 C 8 H 3 Cl 5 O 2 ...
n.o.s. = not otherwise specified meaning a collective entry to which substances, mixtures, solutions or articles may be assigned if a) they are not mentioned by name in 3.2 Dangerous Goods List AND b) they exhibit chemical, physical and/or dangerous properties corresponding to the Class, classification code, packing group and the name and description of the n.o.s. entry [4]
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List of CAS numbers by chemical compound_(Inorganic), Otherwise it confuses readers--124.78.215.110 12:18, 2 May 2009 (UTC) I believe that this article has to be splitted with many in the future, as the collection of CA substance book has not got one but heaps
Name CAS Number InChIKey Descriptors 0 C 12 H 10: Biphenyl 92-52-4 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 1 C 12 H 9 Cl: 2-Chlorobiphenyl 2051-60-7 LAXBNTIAOJWAOP-UHFFFAOYSA-N CP1 2 C 12 H 9 Cl: 3-Chlorobiphenyl 2051-61-8 NMWSKOLWZZWHPL-UHFFFAOYSA-N CP0 3 C 12 H 9 Cl: 4-Chlorobiphenyl 2051-62-9 FPWNLURCHDRMHC-UHFFFAOYSA-N CP0 4 C 12 H 8 Cl 2: 2,2 ...
The current economic method for the production of polyesters is direct esterification of dicarboxylic acids with diols. This condensation polymerization adds monomeric units to a chain. Individual chains react with one another through carboxyl and hydroxyl terminal groups. Finally, transesterification occurs within the chain. [8]