3454-29-3 Usage
Description
1-(2,3-epoxypropoxy)-2,2-bis[(2,3-epoxypropoxy)methyl]butane, also known as Trimethylolpropane Triglycidyl Ether, is a chemical compound characterized by its epoxy groups and versatile molecular structure. It is a colorless to pale yellow liquid with a low viscosity and high reactivity due to the presence of multiple epoxy groups. 1-(2,3-epoxypropoxy)-2,2-bis[(2,3-epoxypropoxy)methyl]butane is known for its ability to form cross-linked polymers and is widely utilized in various industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
1-(2,3-epoxypropoxy)-2,2-bis[(2,3-epoxypropoxy)methyl]butane is used as a key component in the production of pharmaceutical filler complexes. Its application is primarily due to its ability to form stable, cross-linked structures that can enhance the properties of the final product, such as improved mechanical strength, durability, and controlled release of active pharmaceutical ingredients.
The use of Trimethylolpropane Triglycidyl Ether in the pharmaceutical industry is particularly beneficial for the development of drug delivery systems, as it allows for the creation of matrices that can provide a sustained release of medications over time. This can lead to improved patient compliance and more effective treatment outcomes.
Additionally, the compound's reactivity and compatibility with various materials make it a valuable asset in the development of other medical devices and products, such as dental materials, orthopedic implants, and tissue engineering scaffolds.
Check Digit Verification of cas no
The CAS Registry Mumber 3454-29-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3454-29:
(6*3)+(5*4)+(4*5)+(3*4)+(2*2)+(1*9)=83
83 % 10 = 3
So 3454-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O6/c1-2-15(9-16-3-12-6-19-12,10-17-4-13-7-20-13)11-18-5-14-8-21-14/h12-14H,2-11H2,1H3
3454-29-3Relevant articles and documents
BIO-NANO POWER CELLS AND THEIR USES
-
, (2014/01/08)
The present invention concerns bio-nano power cells and methods of their manufacture and use. More particularly, the present invention relates to the preparation of bio-nano power cells that are biocompatible and capable of producing flash, intermittent, or continuous power by electrolyzing compounds in biological systems.
Dendritic polymers with enhanced amplification and interior functionality
-
, (2011/08/03)
Poly(ester-acrylate) and poly(ester/epoxide) dendrimers. These materials can be synthesized by utilizing the so-called “sterically induced stoichiometric” principles. The preparation of the dendrimers is carried out by reacting precursor amino/polyamino-functional core materials with various branch cell reagents. The branch cell reagents are dimensionally large, relative to the amino/polyamino-initiator core and when reacted, produce generation=1 dendrimers directly in one step. There is also a method by which the dendrimers can be stabilized and that method is the reaction of the dendrimers with surface reactive molecules to pacify the reactive groups on the dendrimers.
A facile synthesis of polyglycidyl ethers from polyols and epichlorohydrin
Kida,Yokota,Masuyama,Nakatsuji,Okahara
, p. 487 - 489 (2007/10/02)
The reaction of 1,1,1-tris(hydroxymethyl)ethane (1a), 2-ethyl-2-(hydroxymethyl)-1,3-propanediol (1b), pentaerythritol (1c), or 1,2,6-hexanetriol (1e) with epichlorohydrin in the presence of potassium hydroxide in dimethyl sulfoxide gave the corresponding tri- or tetraglycidyl ethers 3a-c, e in high yields. This procedure was also applicable to the preparation of the phenolic polyglycidyl ethers.