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2-Methylpentane-2,4-diyl diacetate, also known as diacetin, is a colorless liquid chemical compound with the molecular formula C9H18O4. It is classified as a diester and is commonly used in the production of various commercial products, including pharmaceuticals, perfumes, and flavorings. This versatile compound is also utilized as a solvent, plasticizer, and a component in numerous technical and industrial applications. Known for its low toxicity, 2-methylpentane-2,4-diyl diacetate is considered relatively safe for use in a wide range of consumer and industrial products.

1637-24-7

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1637-24-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Methylpentane-2,4-diyl diacetate is used as a solvent and excipient in the pharmaceutical industry for the formulation of medications. Its properties allow for improved solubility and stability of active pharmaceutical ingredients, enhancing the efficacy and safety of various drug formulations.
Used in Perfumery and Flavoring Industry:
In the perfumery and flavoring industry, 2-methylpentane-2,4-diyl diacetate is used as a carrier and solvent for fragrances and flavor compounds. Its ability to dissolve and stabilize these compounds contributes to the creation of long-lasting and consistent scents and tastes in various products.
Used in Technical and Industrial Applications:
2-Methylpentane-2,4-diyl diacetate is employed as a component in technical and industrial applications, such as the production of plastics, resins, and coatings. Its versatility as a solvent and plasticizer allows for the development of innovative materials with improved properties and performance.
Used as a Solvent:
As a solvent, 2-methylpentane-2,4-diyl diacetate is utilized in various chemical processes and reactions, facilitating the dissolution of substances and enabling efficient reactions to take place. Its low toxicity and compatibility with a wide range of materials make it a preferred choice for many applications.
Used as a Plasticizer:
In the plastics industry, 2-methylpentane-2,4-diyl diacetate is used as a plasticizer to increase the flexibility and workability of polymers. Its ability to improve the physical properties of plastics without compromising their integrity makes it a valuable component in the production of various plastic products.

Check Digit Verification of cas no

The CAS Registry Mumber 1637-24-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1637-24:
(6*1)+(5*6)+(4*3)+(3*7)+(2*2)+(1*4)=77
77 % 10 = 7
So 1637-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O4/c1-7(13-8(2)11)6-10(4,5)14-9(3)12/h7H,6H2,1-5H3

1637-24-7SDS

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 (4-acetyloxy-4-methylpentan-2-yl) acetate

1.2 Other means of identification

Product number -
Other names 2,4-diacetoxy-2-methyl-pentane

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:1637-24-7 SDS

1637-24-7Downstream Products

1637-24-7Relevant academic research and scientific papers

Iodine as an Acetyl Transfer Catalyst

Borah, Ruli,Deka, Nabajyoti,Sarma, Jadab C.

, p. 110 - 111 (2007/10/03)

Iodine catalyses the acetylation of amines, phenols and alcohols, including tertiary ones, with acetic anhydride in excellent yield.

Cobalt(II) Chloride Catalyzed Acylation of Alcohols with Acetic Anhydride: Scope and Mechanism

Iqbal, Javed,Srivastava, Rajiv Ranjan

, p. 2001 - 2007 (2007/10/02)

Cobalt(II) chloride catalyzes the acetylation of a variety of alcohols with acetic anhydride in excellent yield.Primary hydroxyl groups can be selectively acylated in the presence of secondary and tertiary ones while the secondary hydroxyl groups can be preferentially acetylated in the presence of tertiary ones.Tertiary alcohols have been found to give ketones, acetoacetates, olefins, and diketene in addition to the acetate.The β-hydroxy esters and ketones can be acylated under these conditions without any elimination, and this reaction has been compared with 4-(dimethylamino)pyridine (DMAP)-mediated acylations where elimination of the resulting β-acetoxy carbonyl compound is observed.A detailed investigation of the acylation of tertiary alcohols has revealed that these reactions proceed via a tertiary alkoxy radical and ketene.A mechanism for these acylations is proposed by invoking an electron-transfer process.

A New Acylation Catalyst

Ahmad, Saeed,Iqbal, Javed

, p. 114 - 115 (2007/10/02)

Cobalt(II) chloride catalyses the acylation of alcohols and amines with anhydrides in excellent yields.

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