5456-05-3 Usage
Uses
Used in Plastics Industry:
Trineopentylglycolbivate is used as a flame retardant for enhancing the fire resistance of various types of plastics. Its application ensures that the plastics maintain their structural integrity and reduce the risk of fire-related incidents.
Used in Textile Industry:
In the textile industry, Trineopentylglycolbivate is utilized as a flame retardant to improve the fire safety of fabrics and garments. This is particularly important for materials used in public spaces, transportation, and protective clothing.
Used in Foams Industry:
Trineopentylglycolbivate is employed as a flame retardant in the production of foams, which are commonly used in furniture, bedding, and insulation. Its incorporation into foams helps to reduce the flammability of these products, thereby increasing their safety for consumer use.
Overall, Trineopentylglycolbivate is an effective and sustainable solution for improving the fire safety of a wide range of materials across different industries, offering a non-toxic and environmentally friendly alternative to conventional flame retardants.
Check Digit Verification of cas no
The CAS Registry Mumber 5456-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5456-05:
(6*5)+(5*4)+(4*5)+(3*6)+(2*0)+(1*5)=93
93 % 10 = 3
So 5456-05-3 is a valid CAS Registry Number.
5456-05-3Relevant academic research and scientific papers
Contribution to the Chemistry of Boron, 228. Synthesis of Structures of (Acyloxy)boranes
Lang, Andreas,Noeth, Heinrich,Schmidt, Martin
, p. 751 - 762 (2007/10/02)
9-Borabicyclononane (9-BBNH) reacts with monocarboxylic acids to afford 9-(acyloxy)-9-borabicyclononanes which are dimers in the solid state as shown by X-ray crystal structures of the benzoate and pivalate.More complex reactions were observed by allowing 9-BBNH to react with dicarboxylic acids in THF or monoglyme.Thus, (9-BBN)2 oxalate 3 contains a fully delocalized oxalate unit with equal C-O and B-O bond lengths.Traces of water convert it into the tetrakis(9-BBN) oxalate 5.A rather unusual structure is veryfied by 9-BBN 2,2-dimethylmalonate 7 which according to its molecular structure is a tetramer featuring a 32-membered ring system.In contrast, reactions of oxalic acid with thexylborane leads to reduction of the acid and formation of a bicyclic dioxaborolo-dioxaborolane 10.Several intermediates were detected by 11B-NMR spectroscopy as well as in reactions of BH3*THF or BH3*SMe2 with oxalic acid. - It follows from the present study that (acyloxy)boranes derived from dicarboxylic acids are strong Lewis acids with an unexpected variety of structural features. - Keywords: Trifluoroacyloxy-9-borabicyclononane / Pivaloyloxy-9-borabicyclononane dimer / Bis(9-borabicyclononyl)oxalate / Tetrakis(9-borabicyclononyl)-dihydroxyoxalate / Bis(9-borabicyclononyl)-2,2-dimethylmalonate tetramer
