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1-[(propoxydisulfanyl)oxy]propane, also known as 1-(propane-1,3-diylbis(sulfanediyl))bis(propan-2-ol), is an organic compound with the chemical formula C6H16O3S2. It is a colorless liquid with a molecular weight of 208.31 g/mol. 1-[(propoxydisulfanyl)oxy]propane is characterized by its two propane-2-ol (propylene glycol) units connected by a disulfide bridge, with each propane-2-ol unit having a propoxy group attached to the sulfur atoms. 1-[(propoxydisulfanyl)oxy]propane is primarily used as a crosslinking agent in the production of polyurethane foams, providing improved mechanical properties and thermal stability to the final product. It is also employed in the synthesis of various chemical intermediates and specialty chemicals. Due to its reactivity and potential hazards, it is essential to handle 1-[(propoxydisulfanyl)oxy]propane with proper safety measures and in accordance with relevant regulations.

3359-05-5

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3359-05-5 Usage

Structure

Propanethiol group bonded to a propylene glycol moiety

Usage

a. Solvent
b. Synthesis of various organic compounds

Odor

Faint

Solubility

Soluble in water

Industrial applications

Wide range of uses

Additional uses

a. Manufacture of pharmaceuticals
b. Agricultural chemicals
c. Other products

Check Digit Verification of cas no

The CAS Registry Mumber 3359-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3359-05:
(6*3)+(5*3)+(4*5)+(3*9)+(2*0)+(1*5)=85
85 % 10 = 5
So 3359-05-5 is a valid CAS Registry Number.

3359-05-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(propoxydisulfanyl)oxypropane

1.2 Other means of identification

Product number -
Other names thiosulfurous acid O,O'-dipropyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3359-05-5 SDS

3359-05-5Downstream Products

3359-05-5Relevant academic research and scientific papers

Synthesis and antimicrobial activities of structurally novel S,S′-bis(heterosubstituted) disulfides

Ramaraju, Praveen,Gergeres, Danielle,Turos, Edward,Dickey, Sonja,Lim, Daniel V.,Thomas, John,Anderson, Burt

experimental part, p. 3623 - 3631 (2012/07/16)

The central focus of this study is on the antibacterial and antifungal properties of synthetically produced S,S′-bis(heterosubstituted) disulfides as a means to control the growth of various infection-causing pathogens. Staphylococcus aureus, Francisella tularensis and Candida albicans were each found to be highly susceptible to several of these compounds by agar or broth dilution and Kirby-Bauer diffusion assays. These structurally simple, low molecular weight disulfides have shown promising bioactivities and may serve as leads to the development of effective new antibacterials for pathogenic bacteria such as methicillin-resistant S. aureus and F. tularensis.

ANTIBACTERIAL S-HETEROSUBSTITUTED DISULFIDES

-

Page/Page column 13, (2009/05/30)

Synthetically-derived S,S-heterodisubstituted disulfides that exhibit potent in vitro antibacterial activity against a variety of bacteria, including Staphylococcus aureus, methicillin-resistant Staphylococcus aureus and Francisella tularensis. The present invention provides compounds, methods and compositions effective to treat microbial/bacterial infections, and, especially, infections arising from bacteria which have developed resistance to conventional antibiotics.

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