3304-97-0 Usage
Uses
Used in Polymer Production:
Tert-butyl dimethyltrithioperoxycarbamate is utilized as a polymerization initiator, playing a crucial role in the production of polymers such as polyethylene and polypropylene. Its reactivity helps in initiating the polymerization process, leading to the formation of these widely used plastics.
Used in Organic Synthesis:
tert-butyl dimethyltrithioperoxycarbamate is also employed in the synthesis of other organic compounds, where its peroxycarbamate functional group can be used to introduce specific chemical functionalities or to facilitate certain reactions.
Used in Agriculture:
Tert-butyl dimethyltrithioperoxycarbamate has been studied for its potential use as a fungicide, indicating its possible application in protecting crops from fungal infections and promoting agricultural productivity.
Used in Antimicrobial Applications:
Additionally, it has been researched for its potential as an antimicrobial agent, suggesting that it could be used to combat microbial growth in various settings, such as in medical or industrial applications.
However, it is important to handle tert-butyl dimethyltrithioperoxycarbamate with care, as its reactivity can pose hazards if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 3304-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3304-97:
(6*3)+(5*3)+(4*0)+(3*4)+(2*9)+(1*7)=70
70 % 10 = 0
So 3304-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NS3/c1-7(2,3)11-10-6(9)8(4)5/h1-5H3
3304-97-0Relevant articles and documents
SYNTHESIS OF MONOFUNCTIONAL THIURAM ACCELERATOR
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Paragraph 0022, (2021/07/02)
The present invention provides a route for synthesizing monofunctional thiuram compounds that is safe, environmentally friendly, and cost effective. This method specifically involves synthesizing a monofunctional thiuram by (1) reacting a tetraorganylthiuram disulfide with an organyl mercaptan to produce the monofunctional thiuram and a dithiocarbamate metal salt or a dithiocarbamate metalloid salt under basic conditions, (2) separating the monofunctional thiuram in an organic phase from the dithiocarbamate metal salt or the dithiocarbamate metalloid salt in an aqueous phase, and (3) recovering the monofunctional thiuram from the aqueous phase. The monofunctional thiuram compounds made in accordance with this invention are of particular value as accelerators for use in the vulcanization of rubber. The use of these monofunctional thiuram compounds as accelerators provides good cure rates and as well as good scorch safety.
