DIMETHYL DISULFIDE

PRODUCT IDENTIFICATION

2930.90

TOXICITY

SMILES

CLASSIFICATION

PHYSICAL AND CHEMICAL PROPERTIES

REFRACTIVE INDEX

APPLICATIONS

• Hydrotreating catalysts
• Initial catalyst improvers
• Sulfur sources
• Catalyst presulfiding
• Natural gas sulfur recovery

Organosulfur compounds are also used in;

• Organic synthesis as organosulfur sources into target organic molecules for the manufacture of pharmaceuticals, adhesives biocides and agricultural products.
• Polymer production
• Lubricant and fuel additives for extreme pressure functionality
• Extraction and reaction solvent
• Metal treatment
• Fungicide

APPEARANCE

ASSAY

99.5% min

COLOR, APHA

30 max

0.3% max

Polarity

The most common solvent is water. Other common solvents which dissolve substances that are insoluble (or nearly insoluble) in water are acetone, alcohol, formic acid, acetic acid, formamide. BTX, carbon disulfide, diemthyl sulfoxide, carbon tetrachloride, chloroform, ether, tetrahydrofuran, furfural, hexane and turpentine. They may be classified as polar and non-polar. Polar solvents, like water, have molecules whose electric charges are unequally distributed, leaving one end of each molecule more positive than the other. Usually polar solvent has O-H bond of which water (HOH), (CH₃OH) and acetic acid (CH₃COOH) are examples. Propanol, butanol, formic acid, formamide are polar solvents. Dipolar solvents which contain a C-O solid bond without O-H bond are acetone [(CH₃)₂C=O], ethyl acetate (CH₃COOCH₂CH₃), methyl ethyl ketone, acetonitrile, N,N-dimethylformamide and diemthyl sulfoxide. Nonpolar solvents, like carbon tetrachloride (CCl₄), benzene (C₆H₆), and diethyl ether ( CH₃CH₂OCH₂CH₃), have molecules whose electric charges are equally distributed and are not miscible with water. Hexane, tetrahydrofuran and methylene chloride are non-polar solvents. Polar solvents are hydrophilic but non-polar solvents are lipophilic. Polar reactants will dissolve in polar solvents. Non-polar solvents dissolve non-polar compounds best. Oil and water don't mix but separate into two layers. There are three measures of the polarity as "dipole moment", "dielectric constant" and "miscibility with water". Though low dipole moments and small dielectric constants indicates non-polar solvents, sharp boundaries between polar and non-polar solvents are not available. The polarity reflects the balance between a polar component (OH) and a non-polar hydrocarbon component, existing in the same molecule. If hydrocarbon character increases relatively, the polarity decreases. On an operational basis, solvents that are miscible with water are polar.

Polar Protic and Dipolar Aprotic

Protic refers to a hydrogen atom attached to an electronegative atom. Protic solvents can donate an H+ (proton) since they contain dissociable H+, such as hydrogen attached to oxygen as in a hydroxyl group, nitrogen as in a amine group. Examples are water, methanol, ethanol, formic acid, hydrogen fluoride and ammonia. Aprotic solvents don't has O-H bond but a C=O bond typically. Examples are acetone [(CH₃)₂C=O] and ethyl acetate (CH₃COOCH₂CH₃). Polar protic solvents are useful in S_N1 reaction, while polar aprotic solvents are S_N2 reaction.