Dipropyl trisulfide

Base Information

• Chemical Name: Dipropyl trisulfide
• CAS No.: 6028-61-1
• Deprecated CAS: 58973-40-3
• Molecular Formula: C6H14S3
• Molecular Weight: 182.375
• European Community (EC) Number: 227-903-4
• UNII: U4529NM2C1
• DSSTox Substance ID: DTXSID5047401
• Nikkaji Number: J99.403K
• Wikidata: Q27290661
• Metabolomics Workbench ID: 45747
• ChEMBL ID: CHEMBL3222023
• Mol file: 6028-61-1.mol

Synonyms:di-n-propyl trisulfide;dipropyl trisulfide

Chemical Property of Dipropyl trisulfide

Chemical Property:

• Appearance/Colour: COA
• Vapor Pressure: 0.0243mmHg at 25°C
• Refractive Index: 1.548
• Boiling Point: 256.8 °C at 760 mmHg
• Flash Point: 106.1 °C
• PSA: 75.90000
• Density: 1.076 g/cm³
• LogP: 3.83600
• Storage Temp.: 2-8°C
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 182.02576397
• Heavy Atom Count: 9
• Complexity: 41.6

Purity/Quality:

99% ^*data from raw suppliers

Dipropyl Trisulfide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 22

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCSSSCCC
• Uses: Dipropyl Trisulfide can be used to determine the antibrowning and antimicrobial effects of onion essential oil to preserve the quality of cut potatoes

Technology Process of Dipropyl trisulfide

There total 30 articles about Dipropyl trisulfide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.9%

phthalimidesulfenyl chloride (54974-07-1) + 1-thiopropane (107-03-9) → phthalimide (136918-14-4,85-41-6) + dipropyl trisulfide (6028-61-1) + N,N'-thiobisphthalimide (7764-29-6)

Guidance literature:

With triethylamine; In chlorobenzene; at 20 ℃;

Reference yield: 62.0%

propyl bromide (106-94-5) → dipropyl trisulfide (6028-61-1)

Guidance literature:

propyl bromide; With Sodium thiosulfate pentahydrate; In ethanol; water; at 20 ℃;

With sodium sulfide nonahydrate; In water; at 0 - 20 ℃; for 6h;

DOI:10.1039/c9cc05562b

Reference yield: 55.1%

1-thiopropane (107-03-9) → dipropyl trisulfide (6028-61-1) + 1,4-di(n-propyl)tetrasulfane (52687-98-6) + Dipropyl disulfide (629-19-6)

Guidance literature:

With boron trifluoride diethyl etherate; sulfur dioxide; In dichloromethane; at 25 ℃; for 24h;

DOI:10.1246/bcsj.56.2657

upstream raw materials:

1-thiopropane

Dimethyldisulphide

Dipropyl disulfide

(disulfido)carbonic acid O-methyl ester SS-propyl ester

Downstream raw materials:

1-benzyl-2-propyldisulfane

benzyl n-propyl trisulfide

1,2-dithiole-3-thione

1-thiopropane

Refernces

• 1、 Chatterjee, Arunavo,Mandal, Niladri Sekhar,Purkayastha, Pradipta. "Selectivity of diallyl trisulfides (DATS) in reducing HAuCl4 to produce gold nanoparticles: a detailed investigation". . . Retrieved 2021/09/08.
• 2、 Sawwan, Nahed,Brzostowska, Edyta M.,Greer, Alexander. "Substituent effects on the reactivity of benzo-1,2-dithiolan-3-one 1-oxides and their possible application to the synthesis of DNA-targeting drugs". . p. 6968 - 6971. Retrieved 2007/10/03.