2801-05-0

Basic information

• Product Name: Carbamodithioic acid, diphenyl-, sodium salt
• CAS NO: 2801-05-0
• Molecular Formula: C13H11NS2.Na
• Molecular Weight: 267.351
• Mol File: 2801-05-0.mol

Chemical Properties

• CAS DataBase Reference: Carbamodithioic acid, diphenyl-, sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamodithioic acid, diphenyl-, sodium salt(2801-05-0)
• EPA Substance Registry System: Carbamodithioic acid, diphenyl-, sodium salt(2801-05-0)

Safety Data

• Hazardous Substances Data: 2801-05-0(Hazardous Substances Data)

Usage

Uses

Used in Rubber and Latex Industry:
Carbamodithioic acid, diphenyl-, sodium salt is used as a vulcanization accelerator for the production of rubber and latex products. It acts as a catalyst in the sulfur vulcanization process, promoting the formation of cross-links between rubber polymer chains, resulting in improved strength, elasticity, and durability of the final product.
Used in Pharmaceutical and Agrochemical Synthesis:
Carbamodithioic acid, diphenyl-, sodium salt is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical properties make it a valuable component in the development of new drugs and agricultural chemicals.
Safety Precautions:
It is important to handle Carbamodithioic acid, diphenyl-, sodium salt with caution due to its potential harmful effects if ingested, inhaled, or comes into contact with the skin. Proper protective equipment, such as gloves, goggles, and masks, should be worn when handling this chemical. Additionally, it should be stored in a cool, dry place away from sources of ignition and incompatible materials to prevent any hazardous reactions.

Upstream product

• 75-15-0 carbon disulfide 
• 122-39-4 diphenylamine 

Downstream Products

• 13575-52-5 C₂₉H₂₇N₃S₄ 
• 847870-04-6 fluoroethyl acetate diphenyldithiocarbamate 
• 548761-45-1 S-(methyl, methyl, acetic acid) dithiocarbamate 
• 230310-02-8 malonate N,N-diphenyl dithiocarbamate 
• 872467-64-6 Fe(II)(pyridine)2(diphenyldithiocarbamato)2 
• 1803-24-3 tetraphenylthiuram disulfide 
• 18509-15-4 C₆H₅SbCl(S₂CN(C₆H₅)2) 
• 1803-09-4 (C₆H₅)2SbS₂CN(C₆H₅)2 
• 18509-24-5 C₆H₅Sb{S₂CN(C₆H₅)2}2 
• 112614-59-2 bis(N,N-diphenyldithiocarbamato)dioxo(triphenylphosphine oxide)uranium(VI) 
• 15683-27-9 copper(II) diphenyldithiocarbamate 
• 428507-13-5 [(PhCH₂)2SnCl(S₂CNPh₂)] 
• 872467-62-4 Mn(II)(pyridine)2(diphenyldithiocarbamato)2 

Relevant articles and documents

Cationic RAFT polymerization using ppm concentrations of organic acid

A metal-free, cationic, reversible addition-fragmentation chain-transfer (RAFT) polymerization was proposed and realized. A series of thiocarbonylthio compounds were used in the presence of a small amount of triflic acid for isobutyl vinyl ether to give p

Photoorganocatalyzed Reversible-Deactivation Alternating Copolymerization of Chlorotrifluoroethylene and Vinyl Ethers under Ambient Conditions: Facile Access to Main-Chain Fluorinated Copolymers

Fluoropolymers have found broad applications for many decades. Considerable efforts have focused on expanding access toward main-chain fluorinated polymers. In contrast to previous polymerizations of gaseous fluoroethylenes conducted at elevated temperatures and with high-pressure metallic vessels, we here report the development of a photoorganocatalyzed reversible-deactivation radical alternating copolymerization of chlorotrifluoroethylene (CTFE) and vinyl ethers (VEs) at room temperature and ambient pressure by exposing to LED light irradiation. This method enables the synthesis of various fluorinated alternating copolymers with low ? and high chain-end fidelity, allowing an iterative switch of the copolymerization between ON and OFF states, the preparation of fluorinated block alternating copolymers, as well as postsynthetic modifications.

Block ethylenic copolymers comprising a vinyllactam block, cosmetic or pharmaceutical compositions containing them and cosmetic use of these copolymers

Disclosed herein are a linear block ethylenic copolymer comprising: at least one block A obtained from monomers comprising from 52% to 99% by weight of at least one ethylenic monomer comprising a lactam ring, of formula (I): and from 1% to 48% by weight o

Block ethylenic copolymers comprising a vinyllactam block, cosmetic or pharmaceutical compositions comprising them and cosmetic use of these copolymers

The present disclosure relates to linear block ethylenic copolymers that have reduced tack and thus do not leave a tacky feel, and to cosmetic and pharmaceutical compositions comprising the linear block ethylenic copolymer. Further disclosed herein is a c