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2,4-DIMETHYL, 1,3-DIOXALONE is a colorless liquid with a dairy aroma and fruity overtones. It has a medium strength odor and is known for its unique chemical properties.

3390-12-3

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3390-12-3 Usage

Uses

Used in Flavor Industry:
2,4-DIMETHYL, 1,3-DIOXALONE is used as a flavoring agent for its dairy aroma with fruity overtones. Its medium strength odor makes it suitable for enhancing the taste and aroma of various food and beverage products.
Used in Fragrance Industry:
In the fragrance industry, 2,4-DIMETHYL, 1,3-DIOXALONE is used as a component in creating various scents due to its unique dairy and fruity aroma. It can be used to add depth and complexity to perfumes, colognes, and other fragrance products.
Used in Chemical Research:
2,4-DIMETHYL, 1,3-DIOXALONE is also utilized in chemical research as a starting material or intermediate for the synthesis of various organic compounds. Its unique structure allows for further modification and exploration of new chemical reactions and applications.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, due to its unique chemical properties, 2,4-DIMETHYL, 1,3-DIOXALONE could potentially be used in the pharmaceutical industry as a building block for the development of new drugs or as a component in drug formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 3390-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3390-12:
(6*3)+(5*3)+(4*9)+(3*0)+(2*1)+(1*2)=73
73 % 10 = 3
So 3390-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O2/c1-4-3-6-5(2)7-4/h4-5H,3H2,1-2H3/t4-,5-/m0/s1

3390-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names EINECS 222-221-3

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:3390-12-3 SDS

3390-12-3Relevant articles and documents

Features of acetal interchange of 1,1-dialkoxyalkanes with 1,2-propylene glycol in neutral solutions

Balashov,Krasnov,Danov,Chernov

, p. 752 - 755 (2001)

Reactions fo 1,1-dimethoxymethane, 1,1-dimethoxyethane, and 1,1-dimethoxypropane with 1,2-propylene glycol at 25°C in neutral solutions were studied by 13C NMR spectroscopy. Under these conditions, 1,1-dimethoxymethane does not react with the g

A study of the oxidehydration of 1,2-propanediol to propanoic acid with bifunctional catalysts

Bandinelli, Claudia,Basile, Francesco,Cavani, Fabrizio,Concepcion, Patricia,De Maron, Jacopo,Dimitratos, Nikolaos,Lambiase, Barbara,Nieto, Jose Manuel Lopez,Tabanelli, Tommaso

, (2019/06/28)

The gas-phase oxidehydration (ODH) of 1,2-propanediol to propionic acid has been studied as an intermediate step in the multi-step transformation of bio-sourced glycerol into methylmethacrylate. The reaction involves the dehydration of 1,2-propanediol into propionaldehyde, which occurs in the presence of acid active sites, and a second step of oxidation of the aldehyde to the carboxylic acid. The two reactions were carried out using a cascade strategy and multifunctional catalysts, made of W-Nb-O, W-V-O and W-Mo-V-O hexagonal tungsten bronzes, the same systems which are also active and selective in the ODH of glycerol into acrylic acid. Despite the similarities of reactions involved, the ODH of 1,2-propanediol turned out to be less selective than glycerol ODH, with best yield to propanoic acid no higher than 13percent, mainly because of the parallel reaction of oxidative cleavage, occurring on the reactant itself, which led to the formation of C1-C2 compounds.

Study on the one-pot oxidative esterification of glycerol with MOF supported polyoxometalates as catalyst

Zhu, Jie,Wang, Peng-Cheng,Lu, Ming

, p. 3383 - 3393 (2015/06/08)

In this work, glycerol was treated under green and mild conditions (water solvent, H2O2 oxidant, 40°C) in an attempt to utilise its additional value. With a metal organic framework (MOF) supported polyoxometallate (POM) as a catalyst, esters were generated as one of the major products which could be useful for various industrial applications. The selectivity of esters formation reached 34.5% in this one-pot oxidative esterification process. Benefiting from the pore limitation effect of the MOF, diffusion was restricted and the original products could be further transformed into esters with the existence of the POM. No other reagents were needed during this process, and all of the intermediates were produced from glycerol itself. The oxidative esterification reaction was studied in detail including the role of the MOF, the influence of pH and the POM type, the mechanism and so on. It was concluded that the POM served as the active site for this oxidative esterification process and H2O2 provided weak acidity in addition to the source of oxygen. Too stronger acidity and oxidizability were unfavourable to the generation of esters. Also, the catalysts could be recovered after reaction, exhibiting good stability and reusability.

Identification of 1,3-dioxanes and 1,3-dioxolanes as malodorous compounds at trace levels in river water, groundwater, and tap water

Romero, Jordi,Ventura, Francesc,Caixach, Josep,Rivera, Josep,Gode, Llui Xavier,Ninerola, Josep Ma.

, p. 206 - 216 (2007/10/03)

A study of organic compounds imparting odor problems in river waters and groundwaters has been conducted. The Tordera aquifer located in Barcelona and Girona (NE Spain) is the water supply reserve for many seasonally crowded villages on the coast. Closed loop stripping analysis (CLSA) and flavor profile analysis (FPA) have been employed as analytical tools to identify the compounds responsible for the odor complaints. The feasibility of purge-and- trap (P and T) has also been evaluated. The 2-alkyl-5,5-dimethyl-1,3-dioxanes and 2-alkyl-4-methyl-1,3-dioxolanes were the most significant compounds identified in river water and groundwater with a threshold odor of 10 ng/L for 2-ethyl-5,5-dimethyl-1,3-dioxane (2EDD), the most malodorous compound. The analyses were carried out by HRGC/MS, and the synthesized 1,3-dioxanes and dioxolanes were characterized by CI-MS and EI-MS/MS techniques. A company, currently manufacturing saturated and unsaturated polyester resins, located in the upper course of the river, produced these compounds as byproducts during the synthesis of resins. The pollution by dioxanes and dioxolanes affected all the aquifer and slowly diminished to the ppt levels when the company was forced to correctly treat their wastewaters. Additional examples of the presence of dioxanes and dioxolanes in wastewaters of other resin plants and also tap water of Barcelona are shown. A study of organic compounds imparting odor problems in river waters and groundwaters has been conducted. The Tordera aquifer located in Barcelona and Girona (NE Spain) is the water supply reserve for many seasonally crowded villages on the coast. Closed loop stripping analysis (CLSA) and flavor profile analysis (FPA) have been employed as analytical tools to identify the compounds responsible for the odor complaints. The feasibility of purge-and-trap (P&T) has also been evaluated. The 2-alkyl-5,5-dimethyl-1,3-dioxanes and 2-alkyl-4-methyl-1,3-dioxolanes were the most significant compounds identified in river water and groundwater with a threshold odor of 10 ng/L for 2-ethyl-5,5-dimethyl-1,3-dioxane (2EDD), the most malodorous compound. The analyses were carried out by HRGC/MS, and the synthesized 1,3-dioxanes and dioxolanes were characterized by CI-MS and EI-MS/MS techniques. A company, currently manufacturing saturated and unsaturated polyester resins, located in the upper course of the river, produced these compounds as byproducts during the synthesis of resins. The pollution by dioxanes and dioxolanes affected all the aquifer and slowly diminished to the ppt levels when the company was forced to correctly treat their wastewaters. Additional examples of the presence of dioxanes and dioxolanes in wastewaters of other resin plants and also tap water of Barcelona are shown.

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