14983-42-7 Usage
Description
Tris(2-methoxyethyl) orthoborate, also known as TMETB, is an organic compound with the chemical formula C9H21BO3. It is a colorless liquid at room temperature and is known for its unique properties, such as its ability to form dynamic polymers with hybrid crosslinked structures. These polymers exhibit a range of characteristics, including damping, cushioning, impact resistance, shape memory, self-repair, and toughness.
Uses
Used in Polymer Industry:
Tris(2-methoxyethyl) orthoborate is used as a monomer for the production of dynamic polymers with hybrid crosslinked structures. These polymers are characterized by their ability to exhibit damping and cushioning properties, making them suitable for applications in shock absorption and vibration damping.
Used in Protective Materials Industry:
Tris(2-methoxyethyl) orthoborate is used as a key component in the development of impact-resistant protective materials. The hybrid crosslinked polymers formed from TMETB provide enhanced resistance to impacts, making them ideal for use in protective gear and equipment.
Used in Shape Memory Materials Industry:
Tris(2-methoxyethyl) orthoborate is utilized as a precursor in the creation of shape memory materials. These materials have the ability to return to their original shape after being deformed, making them useful in various applications, such as medical devices and smart textiles.
Used in Self-Repairing Materials Industry:
Tris(2-methoxyethyl) orthoborate is employed as a building block for self-repairing materials. The dynamic nature of the hybrid crosslinked polymers allows them to heal themselves when damaged, making them highly desirable for applications where durability and longevity are crucial.
Used in Tough Materials Industry:
Tris(2-methoxyethyl) orthoborate is used as a component in the formulation of tough materials. The hybrid crosslinked polymers derived from TMETB exhibit increased toughness, making them suitable for use in various industrial applications where resistance to wear and tear is essential.
Check Digit Verification of cas no
The CAS Registry Mumber 14983-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,8 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14983-42:
(7*1)+(6*4)+(5*9)+(4*8)+(3*3)+(2*4)+(1*2)=127
127 % 10 = 7
So 14983-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H21BO6/c1-11-4-7-14-10(15-8-5-12-2)16-9-6-13-3/h4-9H2,1-3H3
14983-42-7Relevant articles and documents
FT-IR and NMR study of tris(oxaalkyl) borates and their complexes with HAuCl4
Brzezinski,Gierczyk,Rózalski,Wojciechowski,Schroeder,Zundel
, p. 119 - 123 (2000)
Three tris(oxaalkyl) borates and their complexes with HAuCl4 were studied by FT-IR, 1H and 13C NMR spectroscopy. Continuous absorption in the FT-IR spectra of the complexes testifies the formation of proton channels showing large proton polarizability. The shape of the proton potential is discussed on the basis of the NM -data. (C) 2000 Elsevier Science B.V.
Multinuclear NMR studies of tris(oxaalkyl) borates and their complexes with some metal cations
Gierczyk,Schroeder,Nowak-Wydra,Wojciechowski,Brzezinski
, p. 149 - 153 (1999)
Nuclear magnetic resonance (NMR) of 1H, 13C, 11B and 17O nuclei has been used for the study of complexation of CoCl2, NiCl2 and CuCl2 salts with three tris(oxaalkyl) borates. All NMR techniques demonstrated the formation of complexes but the most informative were the 13C and 17O NMR measurements. The structures of the complexes formed are discussed in this article.
TRICYANOBORATE ALKYL ETHERS
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Page/Page column 21, (2014/03/26)
The invention relates to tricyanoborate alkyl ethers, a method for their preparation and their use as ionic liquids.
