What is the Butyl disulfide?

Butyl disulfide is clear colourless to very slightly brown liquid, while it's Molecular Formula is C8H18S2 . clear colourless to very slightly brown liquid

What is the CAS number for Butyl disulfide?

The CAS number of Butyl disulfide is 629-45-8.

What is the Butyl disulfide?

Butyl disulfide is clear colourless to very slightly brown liquid, while it's Molecular Formula is C8H18S2 . clear colourless to very slightly brown liquid

What is the CAS number for Butyl disulfide?

The CAS number of Butyl disulfide is 629-45-8.

Detailed introduction

99% Purity Commercial production n-Butyl disulfide 629-45-8 with Cheapest Price

Molecular Formula:C8H18S2
Molecular Weight:178.363
Appearance/Colour:clear colourless to very slightly brown liquid
Vapor Pressure:52 mm Hg ( 37.7 °C)
Melting Point:-94 °C
Refractive Index:n20/D 1.492(lit.)
Boiling Point:226 °C at 760 mmHg
Flash Point:93.3 °C
PSA：50.60000
Density:0.946 g/cm³
LogP:3.96800

Butyl disulfide(Cas 629-45-8) Usage

Synthesis Reference(s)	Chemical and Pharmaceutical Bulletin, 34, p. 486, 1986 DOI: 10.1248/cpb.34.486Synthesis, p. 1091, 1982 DOI: 10.1055/s-1982-30083
Purification Methods	Shake it with lead peroxide, filter and distil it in a vacuum under N2. [Beilstein 1 IV 1560.]

InChI:InChI=1/C8H18S2/c1-3-5-7-9-10-8-6-4-2/h3-8H2,1-2H3

629-45-8 Relevant articles

Synthesis and Characterization of "atlas-Sphere" Copper Nanoclusters: New Insights into the Reaction of Cu2+ with Thiols

Cook, Andrew W.,Jones, Zachary R.,Wu, Guang,Teat, Simon J.,Scott, Susannah L.,Hayton, Trevor W.

, p. 8739 - 8749 (2019)

Thiolates are a widely used ligand class...

METAL COMPLEXES OF TETRAPYRAZINOPORPHYRAZINES - EFFECTIVE CATALYSTS OF THE OXIDATION OF MERCAPTANS

Maizlish, V. E.,Korzhenevskii, A. B.,Klyuev, V. N.

, p. 1031 - 1033 (1984)

The catalytic activity of the tetrapyraz...

Rearrangement of radicals with migration of the chlorine atom from sulfur to carbon during the reaction of thiols with vinylsulfonyl chloride

Kandror,Freidlina

, p. 1814 - 1816 (1975)

1. A study was made of the reaction of n...

Synergistic Effect of Iodine and Neighboring Amine Groups on Thioester Deacylation

Doi, Joyce Takahashi,Carpenter, Tracy Louise,Olmstead, Marylin M.,Musker, W. Kenneth

, p. 4684 - 4689 (1983)

The synergistic effect of a Lewis acid (...

Visible-light-responsive lanthanide coordination polymers for highly efficient photocatalytic aerobic oxidation of amines and thiols

An, Shuyi,Guo, Zhifen,Liu, Xin,Che, Yan,Xing, Hongzhu,Chen, Peng

, p. 15767 - 15775 (2021/09/22)

Development of visible-light-induced pho...

Trisulfides over disulfides: Highly selective synthetic strategies, anti-proliferative activities and sustained H2S release profiles

Bhattacherjee, Debojit,Sufian, Abu,Mahato, Sulendar K.,Begum, Samiyara,Banerjee, Kaustav,De, Sharmistha,Srivastava, Hemant Kumar,Bhabak, Krishna P.

supporting information, p. 13534 - 13537 (2019/11/14)

Temperature-and solvent-induced selectiv...

T BuOK-triggered bond formation reactions

Xu, Yulong,Shi, Xiaonan,Wu, Lipeng

, p. 24025 - 24029 (2019/08/13)

Recently, inexpensive and readily availa...

629-45-8 Process route

: 7315-50-6
α,α-bis(butylthio)toluene

: 629-45-8
dibutyl disulfide

: 100-52-7
benzaldehyde

Conditions

Conditions	Yield
With water; 1-fluoro-2,4,6-trimethylpyridinium trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane; at 23 ℃; Mechanism; other acyclic dithioacetal (R=Ph);	80%