7580-12-3 Usage
Description
2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE is a chemical compound with the molecular formula C12H24O3. It is an organic compound that consists of a trioxane ring with three propyl groups attached to it. 2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE is known for its versatile applications across various industries due to its unique chemical structure and properties.
Uses
Used in Adhesives and Coatings Industry:
2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE is used as a crosslinking agent for the production of epoxy resins, which are essential components in the formulation of high-performance adhesives and coatings. Its ability to form strong crosslinks enhances the durability, chemical resistance, and mechanical properties of the final products.
Used in Electronic Materials Industry:
In the electronic materials industry, 2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE serves as a crosslinking agent in the production of epoxy resins used for encapsulation and potting of electronic components. This helps protect the components from environmental factors, such as moisture and chemicals, and ensures their reliable performance.
Used in Polyurethane Foam Manufacturing:
2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE is used as a curing agent in the manufacturing of polyurethane foams. Its presence accelerates the reaction between isocyanates and polyols, resulting in the formation of a stable foam structure with desirable properties, such as low density, good mechanical strength, and excellent thermal insulation.
Used in Plasticizers Production:
2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE is also utilized in the production of plasticizers, which are additives used to increase the flexibility and workability of various types of plastics. 2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE contributes to the development of plasticizers with improved performance characteristics, such as enhanced compatibility with polymers and reduced volatility.
Used in Pharmaceutical Industry:
2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE has potential applications in the pharmaceutical industry, where it can be used as an intermediate in the synthesis of various drug molecules. Its unique structure and reactivity make it a valuable building block for the development of new pharmaceutical compounds.
Used as a Specialty Chemicals Solvent:
In the field of specialty chemicals, 2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE serves as a solvent for various applications. Its ability to dissolve a wide range of substances makes it suitable for use in processes that require the dissolution or extraction of specific compounds.
However, it is crucial to handle 2,4,6-TRIPROPAN-2-YL-1,3,5-TRIOXANE with caution, as it may pose health and environmental risks if not used properly. Proper safety measures and disposal methods should be followed to minimize any potential hazards associated with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 7580-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,8 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7580-12:
(6*7)+(5*5)+(4*8)+(3*0)+(2*1)+(1*2)=103
103 % 10 = 3
So 7580-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O3/c1-7(2)10-13-11(8(3)4)15-12(14-10)9(5)6/h7-12H,1-6H3
7580-12-3Relevant articles and documents
Beryllium-Induced Conversion of Aldehydes
Müller, Matthias,Buchner, Magnus R.
, p. 11147 - 11156 (2019/08/12)
Aldehydes play a key role in the human metabolism. Therefore, it is essential to know their reactivity with beryllium compounds in order to assess its effects in the body. The reactivity of simple aldehydes towards beryllium halides (F, Cl, Br, I) was studied through solution and solid-state techniques and revealed distinctively different reactivities of the beryllium halides, with BeF2 being the least and BeI2 the most reactive. Rearrangement and aldol condensation reactions were observed and monitored by in situ NMR spectroscopy. Crystal structures of various compounds obtained by Be2+-catalyzed cyclization, rearrangement, and aldol addition reactions or ligation of beryllium halides have been determined, including unprecedented one-dimensional BeCl2 chains and the first structurally characterized example of an 1-iodo-alkoxide. Long-term studies showed that only aldehydes without a β-H can form stable beryllium complexes, whereas other aldehydes are oligo- and polymerized or decomposed by beryllium halides.
Novel acidic ionic liquids as efficient and recyclable catalysts for the cyclotrimerization of aldehydes
Song, Heyuan,Chen, Jing,Xia, Chungu,Li, Zhen
experimental part, p. 266 - 273 (2011/10/31)
A mild, efficient, and ecofriendly procedure for cyclotrimerization of aldehydes was realized by using a series of novel Brnsted acidic ionic liquids (BAILs) consisting of double-SO3H groups in cations as catalysts. Good conversion of aldehydes and selectivity of trialkyl-1,3,5-trioxanes were achieved by using 1mol% of BAILs. In addition, the catalyst system could be recycled and reused at least eight times without apparent loss of activity. Taylor & Francis Group, LLC.
InCl3 as an efficient catalyst for cyclotrimerization of aldehydes: Synthesis of 1,3,5-Trioxane under solvent-free conditions
Elamparuthi,Ramesh,Raghunathan
, p. 2801 - 2804 (2007/10/03)
1,3,5-Trioxanes derived from aldehydes were synthesized using indium trichloride as a catalyst. Cyclotrimerization of the aldehydes gave excellent yields under neat conditions within a short span of time. Copyright Taylor & Francis, Inc.