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1119-40-0

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1119-40-0 Usage

General Description

Different sources of media describe the General Description of 1119-40-0 differently. You can refer to the following data:
1. Dimethyl glutarate, also known as glutaric acid dimethyl ester, dimethyl ester, pentanedioic acid, or dimethyl pentanedioate is an organic chemical with the molecular formula C7H12O4. It has a faint agreeable odor and is very soluble in alcohol and ether.
2. Colorless liquid.

Uses

Different sources of media describe the Uses of 1119-40-0 differently. You can refer to the following data:
1. Industrial Uses Dimethyl glutarate is used as an intermediate and solvent in the packing and formulation of mixtures and substances. It is also used as an intermediate in the manufacture of cleaning agents, lubricants, coating agents, rolling oils, metal working fluids, blowing agents, functional fluids. The compound is used in laboratories, polymer processing, water treatment chemicals, rubber production and processing. Uses by professional Workers Dimethyl glutarate is used in gas and oil field production and drilling operations. It is used in de-icing and anti-icing applications, construction and road applications, and release and binders agents. Consumer Uses The compound is used in the manufacture of agrochemicals and water treatment chemicals.
2. Dimethyl glutarate is applied as paint and graffiti removers, nail polish removers, hand cleaners, adhesives, sealants and caulks, automotive cleaning products, bathroom and tile cleaners, general purpose cleaners, spot removers, floor maintenance products.

Chemical Properties

CLEAR COLOURLESS LIQUID

Synthesis Reference(s)

Synthesis, p. 555, 1985 DOI: 10.1055/s-1985-31275

Air & Water Reactions

Flammable. Hydrolyzed by strong mineral acids and strong alkalis.

Reactivity Profile

Glutaric acid dimethyl ester is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 1119-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1119-40:
(6*1)+(5*1)+(4*1)+(3*9)+(2*4)+(1*0)=50
50 % 10 = 0
So 1119-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c1-7-8-5-6-11-9(8)3-4-10(7)12-2/h3-6,11H,1-2H3

1119-40-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B24359)  Dimethyl glutarate, 98%   

  • 1119-40-0

  • 25g

  • 185.0CNY

  • Detail
  • Alfa Aesar

  • (B24359)  Dimethyl glutarate, 98%   

  • 1119-40-0

  • 100g

  • 315.0CNY

  • Detail
  • Alfa Aesar

  • (B24359)  Dimethyl glutarate, 98%   

  • 1119-40-0

  • 500g

  • 1245.0CNY

  • Detail
  • Aldrich

  • (D158801)  DBE-5dibasicester  99%

  • 1119-40-0

  • D158801-100G

  • 607.23CNY

  • Detail

1119-40-0SDS

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 Glutaric acid dimethyl ester

1.2 Other means of identification

Product number -
Other names Pentanedioic acid, dimethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Solvents
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:1119-40-0 SDS

1119-40-0Relevant articles and documents

-

Schaafsma,S.E. et al.

, p. 827 - 830 (1973)

-

Hagedorn III,Farnum

, p. 3765 (1977)

Straightforward synthesis of functionalized (E)-3-acylacrylic acids

Sivák, Ivan,Václav, Jakub,Berke?, Du?an,Kolarovi?, Andrej

, p. 8871 - 8875 (2015)

An experimentally simple, mild and straightforward synthetic route towards diversely functionalized (E)-3-acylacrylic acids is described, with Horner-Wadsworth-Emmons (HWE) reaction as the key step. The substrate scope and limitations of the HWE reaction were investigated with a range of β-ketophosphonates. Glyoxylic acid monohydrate was demonstrated to be fully compatible with the HWE reaction conditions, thus avoiding a troublesome hydrolysis of the corresponding 3-acylacrylates in the last step and providing a valuable synthetic shortcut.

Sulfonic acid-functionalized organic knitted porous polyaromatic microspheres as heterogeneous catalysts for biodiesel production

Varyambath, Anuraj,Kim, Mi-Ra,Kim, Il

, p. 12745 - 12753 (2018/08/04)

The use of renewable energy sources decreases the consequences of greenhouse gas emission from fossil fuels. Biodiesel, an easily burning and biodegradable fuel, is an alternative to conventional diesel fuel. The esterification of long-chain fatty acids and transesterification of triglycerides are two major reactions widely used to convert vegetable oils or animal fats into biodiesel. As solid acid catalysts are considered promising candidates for biodiesel production, we have synthesized a series of organic knitted porous polyaromatics (OPPs) using pyrene, anthracene, and naphthalene as monomers via Friedel-Crafts alkylation, followed by crosslinking reactions. The resultant polymers showed good surface morphology, stability and swelling property, high capacity for functionalization due to the unreacted bromomethyl groups on the surface, and excellent hydrophobicity. The sulfonated polymer microspheres obtained by the surface sulfonation showed good surface acidity; thus, they can be employed as heterogeneous solid acid catalysts for the esterification of long-chain fatty acids and transesterification of triglycerides, and they are reusable without any leaching of functional groups.

Efficient and selective oxidation of aldehydes with dioxygen catalysed by vanadium-containing heteropolyanions

El Amrani, Ikram,Atlamsani, Ahmed,Dakkach, Mohamed,Rodríguez, Montserrat,Romero, Isabel,Amthiou, Souad

, p. 888 - 895 (2017/09/26)

The heteropolyacids “H3+n[PMo12–nVnO40]·aq” (denoted as HPA-n; n = 2, 3, 8) catalyse the oxidation of aldehydes to carboxylic acids in the presence of dioxygen with very good yields. The effect on the catalytic activity of various parameters such as the precursors, solvent, temperature or catalyst/substrate ratio was examined. The process is particularly selective for linear and aromatic aldehydes. The oxidation of adipaldehyde with dioxygen in mild conditions, in the presence of HPA-2 as a catalyst, leads to the formation of adipic acid together with a significant amount of other byproducts. Thus, several modifications of the catalytic systems have been carried out to improve their selectivity. The effect of cocatalysts was investigated and, among the species tested, complex Ni(acac)2 was found to be the most efficient yielding 60% of adipic acid.

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