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Isopropyl hydrogen maleate, also known as isopropyl maleate or 2-methylprop-2-enoic acid, is an organic compound with the chemical formula C6H8O4. It belongs to the class of maleates, which are esters of maleic acid. This colorless, odorless liquid is flammable and requires careful handling and storage to prevent hazards from mishandling or exposure to incompatible substances.

924-83-4

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924-83-4 Usage

Uses

Used in Plastics Industry:
Isopropyl hydrogen maleate is used as a plasticizer and a monomer for the production of various types of plastics. It enhances the flexibility and processability of plastic materials, making them more suitable for various applications.
Used in Resin Industry:
In the resin industry, isopropyl hydrogen maleate is used as a raw material for the synthesis of resins. It contributes to the formation of resins with specific properties, such as adhesion, flexibility, and chemical resistance, which are essential for various industrial applications.
Used in Adhesive Industry:
Isopropyl hydrogen maleate is used as a component in the formulation of adhesives. It improves the adhesive properties, such as bond strength and durability, making the adhesives more effective in joining different materials.
Used in Organic Synthesis:
Isopropyl hydrogen maleate is used as a starting material or an intermediate in the synthesis of other organic compounds. Its reactive double bond allows for various chemical reactions, leading to the formation of a wide range of products with different applications in industries such as pharmaceuticals, agrochemicals, and dyes.

Check Digit Verification of cas no

The CAS Registry Mumber 924-83-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 924-83:
(5*9)+(4*2)+(3*4)+(2*8)+(1*3)=84
84 % 10 = 4
So 924-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O4/c1-5(2)11-7(10)4-3-6(8)9/h3-5H,1-2H3,(H,8,9)/b4-3-

924-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-4-oxo-4-propan-2-yloxybut-2-enoic acid

1.2 Other means of identification

Product number -
Other names maleic acid-monoisopropyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:924-83-4 SDS

924-83-4Downstream Products

924-83-4Relevant academic research and scientific papers

SUBSTITUTED 3-ISOBUTYL-9,10-DIMETHOXY-1,3,4,6,7,11B-HEXAHYDRO-2H-PYRIDO[2,1-a]ISOQUINOLIN-2-OL COMPOUNDS, THEIR SYNTHESIS, AND USE THEREOF

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Paragraph 0152-0153, (2021/04/02)

The invention relates to substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-2-ol compounds, their synthesis, pharmaceutical compositions containing them, and methods of using them in the treatment of disorders benefiting from inhibition of vesicular monoamine transporter 2 (VMAT2).

Synthesis of α,β-unsaturated esters of perfluoropolyalkylethers (PFPAEs) based on hexafluoropropylene oxide units for photopolymerization

Bonneaud, Céline,Decostanzi, Mélanie,Burgess, Julia,Trusiano, Giuseppe,Burgess, Trevor,Bongiovanni, Roberta,Joly-Duhamel, Christine,Friesen, Chadron M.

, p. 32664 - 32671 (2018/10/15)

α,β-unsaturated esters are usually synthesized for polymer applications. However, the addition of maleate (cis-configuration) to a fluorinated moiety is challenging due to its potential isomerization during esterification. Various synthetic routes were attempted and led to very low conversion or side-products. The immiscibility of both reagents combined with an easy isomerization or attack on the double bond were potential explanations. In this paper, the synthesis of maleates oligo(hexafluoropropylene oxide) is reported by Steglich esterification and the reaction conditions are discussed depending on the molecular weight of the fluorinated moieties. After UV-curing, hydrophobic polymers were obtained by copolymerization with vinyl ethers by electron acceptor-donor systems.

Metal salts of hydrolyzed olefin/maleic anhydride copolymers and their use as wood preservatives

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Page/Page column 19-20, (2009/06/27)

Complexes of copper and/or zinc with hydrolyzed olefin/maleic anhydride copolymers were solubilized in ammoniacal solution providing preservative solutions that fully penetrate wood. With loss of the ammonia from the wood, the complexes were stably retained in the wood providing a long lasting preservative.

Ring-opening of cyclic anhydrides using ionic liquids

Jiang, Dong,Wang, Yuan Yuan,Xu, Yan Nan,Dai, Li Yi

experimental part, p. 167 - 169 (2009/10/15)

Four novel Bronsted acidic ionic liquids with two different acid sites on the imidazolium cations were synthesised and employed as catalysts and solvents for the ring-opening of cyclic anhydrides to synthesise half-esters. The results showed that these novel Bronsted acidic ionic liquids were efficient and recyclable. Good yields, short reaction times and mild reaction conditions were achieved.

Ibuprofen complexes as wood preservatives

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Page/Page column 11, (2009/01/20)

Complexes of ibuprofen and copper and/or zinc were solubilized in ammoniacal solution providing preservative solutions that fully penetrate wood. With loss of the ammonia from the wood, the complexes were stably retained in the wood providing a long lasting preservative.

TROPOLONE COMPLEXES AS WOOD PRESERVATIVES

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Page/Page column 25, (2008/06/13)

Complexes of tropolone and copper and/or zinc were solubilized in ammoniacal solution providing preservative solutions that fully penetrate wood. With loss of the ammonia from the wood, the complexes were stably retained in the wood providing a long lasting preservative.

Fumaric acid derivative and polymer therefrom

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, (2008/06/13)

A polymer obtained by polymerizing a fumaric acid derivative represented by the following general formula (1): STR1 in which R1 represents an alkyl group having 1-6 carbon atoms and A denotes a radical of STR2 in which R2 and R3 represent each an alkyl group having 1-4 carbon atoms and may be identical with or different from each other, R4 denotes an alkyl group having 1-6 carbon atoms or a benzyl group and m and n denote each an integer of 1-6.

A new simplified method for esterification of secondary and tertiary alcohols

Kammoun,Le Bigot,Delmas,Boutevin

, p. 2777 - 2781 (2007/10/03)

Esters of secondary and tertiary alcohols have been synthetized in the absence of solvent and catalyst and only under the effect of temperature with high yields.

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