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Di-sec-butyl fumarate, also known as 1,4-butanediyl bis(2-methylpropanoate), is an organic compound with the chemical formula C12H20O4. It is a colorless to pale yellow liquid with a fruity, green, and slightly ester-like odor. This ester is formed by the reaction of fumaric acid with di-sec-butyl alcohol and is commonly used as a fragrance ingredient in various personal care products, such as perfumes, soaps, and lotions. Di-sec-butyl fumarate is also employed as a solvent and a plasticizer in the manufacturing of plastics and resins. It is considered to be relatively stable and non-toxic, but like many chemicals, it should be handled with care to avoid potential health and environmental risks.

2210-32-4

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2210-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2210-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2210-32:
(6*2)+(5*2)+(4*1)+(3*0)+(2*3)+(1*2)=34
34 % 10 = 4
So 2210-32-4 is a valid CAS Registry Number.

2210-32-4SDS

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 dibutan-2-yl but-2-enedioate

1.2 Other means of identification

Product number -
Other names DI-SEC-BUTYL FUMARATE

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:2210-32-4 SDS

2210-32-4Relevant academic research and scientific papers

Efficient synthesis of symmetrical phthalate and maleate diesters using phosphinite ionic liquids

Valizadeh,Khalili

, p. 529 - 534 (2013/02/22)

Symmetrical dialkyl phthalates and maleates were synthesized using phosphinite ionic liquid as a catalyst and reaction medium. The results indicated that phosphinite ionic liquid shows better catalytic and reusable performance without using any acid or base catalyst. Under the optimum conditions, using 1-methyl-3-(4-phosphinitebutyl) imidazolium chloride as catalyst, the conversion of phthalic and maleic anhydrides to the corresponding diesters of primary and secondary alcohols was occurred in 72-85% yields. The diesters of tertiary alcohols and phenols could not be prepared by this method. A kind of widely used plasticizer, dioctyl phthalate, was prepared in good yield under these conditions. The ionic liquid could be reused three times after easy separation from the products without any disposal. Iranian Chemical Society 2012.

Unsaturated mono-esters and their use in coating compositions

-

, (2008/06/13)

Hydroxy functional, unsaturated diesters are disclosed that comprise the esterification reaction products of unsaturated anhydrides with secondary alcohols to form monoesters, followed by oxyalkylation of the monoester with epoxy compounds, whereby a diester is formed with hydroxy functionality. Use of secondary alcohol yields monoesters less prone to disproportionation. The unsaturated diesters may be copolymerized with vinyl monomers to form hydroxy functional copolymers useful in coating applications, wherein they may be included in compositions along with a curing agent that is reactive with hydroxy groups.

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