N-Heptyl mercaptan

HEPTANOL 5-HETHYL-l-HEXANOL ISOPROPYL-TERT-BUTYL-ETHER n-HEPTYL MERCAPTAN BUTYL-PROPYL-SULFIDE ETHYL-PENTYL-SULFIDE HEXYL-METHYL-SULFIDE... 

Methyl mercaptan Ethyl mercaptan Propyl mercaptan wo-Propyl mercaptan Butyl mercaptan. wo-Butyl mercaptan j c-Butyl mercaptan ferf-Butyl mercaptan Amyl mercaptan 5 ec-Amyl mercaptan wo-Amyl mercaptan ten-Amy mercaptan n-Hexyl mercaptan n-Heptyl mercaptan n-Octyl mercaptan 5 oc-Octyl mercaptan n-Nonyl mercaptan forf-Nonyl mercaptan n-Decyl mercaptan Undecyl mercaptan n-Dodecyl mercaptan ten-DodocyX mercaptan fn-wo-Butyl mercaptan Phenyl mercaptan Benzyl mercaptan li-Limonene mercaptan Perchloromethyl mercaptan 3-Methyl- 1-butanethiol 2-Mercaptoethanol... 

C7H16S n-HEPTYL MERCAPTAN 59.314 4.3814E-01 8.8964E-05 -2.6174E-07 8.7398E-11 200 1500... 

Synonyms/Trade Names Heptyl mercaptan, n-Heptyl mercaptan ... 

Synonyms n-Heptanethiol Heptyl mercaptan 1-Heptyl mercaptan n-Heptyl mercaptan n-Heptylthiol n-Thioheptyl alcohol Classification Sat. thioalcohol Empirical C7H16S... 

In our initial attempts to study the effect of (DODA) Chloride, (DODA)C, sonicated vesicles on the thiolysis of p-nitrophenylacetate (NPA) by n-heptyl mercaptan (HM) we found that metal from the probe catalyzed the oxidation of the mercaptan [Cuccovia, I.M., unpublished]. In order to avoid mercaptan oxidation we developed an alcohol injection method for the preparation of (DODA)C vesicles, that were characterized by gel filtration and by the incorporation of lipid soluble probes [15]. It is not clear, today, if the aggregates prepared by ethanol injection are highly permeable closed vesicles or other types of bilayer assemblies [16]. 

Table 11. Solubility and Solubilization of Organic Molecules (Monomers and n-Heptyl Mercaptan) in Water and Surfactant Solutions, Respectively ...

If a higher thiol, e.g. n-hexyl or n-heptyl mercaptan is used with piperidine then in about 24 hours at room temperature disulphide links are also cleaved. The use of the thiol-amine system thus allows polysulphide and disulphide links to be distinguished. The reaction times are also much shorter than with triphenyl phosphine in which typical reactions take about 96 hours at 80°C. 

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