T58408
Triethanolamine borate
97%
Synonym(s):
2,2′,2′′-Nitrilotriethyl borate, Boratrane
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About This Item
Empirical Formula (Hill Notation):
C6H12BNO3
CAS Number:
Molecular Weight:
156.98
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
206-003-5
Beilstein/REAXYS Number:
774536
MDL number:
Product Name
Triethanolamine borate, 97%
InChI key
NKPKVNRBHXOADG-UHFFFAOYSA-N
InChI
1S/C6H12BNO3/c1-4-9-7-10-5-2-8(1)3-6-11-7/h1-6H2
SMILES string
C1CN2CCOB(O1)OCC2
assay
97%
form
powder
mp
235-237 °C (lit.)
Quality Level
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Application
Triethanolamine borate can be used:
- As a surface stabilizing electrolyte additive for Ni-rich layered oxide cathode. TEAB inhibits Ni dissolution in the Ni-rich cathode and suppresses the electrolyte decomposition.
- To prepare highly crystalline wide band gap perovskite solar cells with enhanced efficiency. TEBA helps to slow down the rapid crystallization and facilitates the formation of uniform perovskite films with reduced defects.
- As a bifunctional catalyst for the cycloaddition of CO2 with epoxides.
- As a precursor to synthesize boron-containing epoxy resin with flameretardant properties.
Features and Benefits
- Water-Soluble and Eco-Friendly: Easily dissolves in water, is non-toxic, and environmentally benign, making it suitable for green chemistry applications
- Thermal Stability and Flame Retardancy: Offers excellent chemical and thermal stability, and serves as a flame retardant in plastics and textiles
- Easy Removal and Processing
General description
Triethanolamine borate (TEAB) is a water-soluble, eco-friendly boron-containing coordination compound synthesized from triethanolamine and boric acid, featuring a Lewis pair structure (boron as Lewis acid, amine as Lewis base). TEAB serves as a versatile additive and catalyst in polymer chemistry, lubrication, and energy storage, owing to its thermal stability, flame-retardant properties, and ability to enhance ionic conductivity. Its compatibility with organic matrices and non-toxic profile make it ideal for applications in flame-retardant materials, high-performance lubricants, solid-state electrolytes, and as a corrosion inhibitor. These attributes have led to its widespread use in catalysis, lithium-ion secondary batteries, and advanced polymer systems.
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Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of a novel boron-containing hyperbranched benzoxazine and its flame-retardant properties in copolymer with epoxy resin
Jia-Xin Cheng, et al.
Polymers For Advanced Technologies, 34, 2694-2706 (2023)
Synthesis of a novel boron-containing hyperbranched benzoxazine and its flame-retardant properties in copolymer with epoxy resin
Jia-Xin Cheng, et al.
Polymers For Advanced Technologies, 34, 2694-2706 (2023)
Triethanolamine borate as bifunctional Lewis pair catalyst for the cycloaddition of CO2 with epoxides
Yuansheng Ge, et al.
Journal of CO2 Utilization, 57, 101873-101873 (2022)
Triethanolamine borate as a surface stabilizing bifunctional additive for Ni-rich layered oxide cathode
Sang Hoo Lim, et al.
International Journal of Energy Research, 45, 2138-2147 (2021)
A Bermúdez et al.
Journal of cell science, 111 ( Pt 12), 1707-1715 (1998-05-28)
To examine the internal structure of chromatin fibers, we have developed procedures for partial denaturation of small chromatin fragments (8-30 nucleosomes) from chicken erythrocytes. Electron micrographs of samples prepared under conditions that cause nucleosome dissociation show rods and loops projecting
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