Triphenylmethyl mercaptan, 98+%, Thermo Scientific Chemicals
Triphenylmethyl mercaptan, 98+%, Thermo Scientific Chemicals
Triphenylmethyl mercaptan, 98+%, Thermo Scientific Chemicals
Triphenylmethyl mercaptan, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Triphenylmethyl mercaptan, 98+%, Thermo Scientific Chemicals

CAS: 3695-77-0 | C19H16S | 276.397 g/mol
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Catalog NumberQuantity
ALFA14888.065 g
Catalog number ALFA14888.06
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Quantity:
5 g
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Specifications
Chemical Name or MaterialTriphenylmethyl mercaptan
CAS3695-77-0
Health Hazard 1H332
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P271-P304+P340-P312
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Triphenylmethyl mercaptan, is used as a reagent used for the introduction of thiol group. Triphenylmethanethiol is a reagent used for the mild introduction of the mercapto functionality. It is also used as a pharmaceutical intermediate; Chemical synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Triphenylmethyl mercaptan, is used as a reagent used for the introduction of thiol group. Triphenylmethanethiol is a reagent used for the mild introduction of the mercapto functionality. It is also used as a pharmaceutical intermediate; Chemical synthesis.

Solubility
It is insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents. Stable under recommended storage conditions.
RUO – Research Use Only

General References:

  1. Norman Kharasch.; Homer R. Williams. A Catalytic Synthesis of Triphenylmethyl Mercaptan. J. Am. Chem. Soc. 1950, 72, (4), 1843-1844.
  2. Convenient reagent for the introduction of the thiol group. The trityl group can be cleaved with Ag(I) or Hg(II) salts: J. Am. Chem. Soc., 104, 1391 (1982).