Triethanolaminoborate
orthoboric acid, compound with 2,2',2''-nitrilotriethanol
CAS: 10049-36-2
Molecular Formula: C6H15NO3.xBH3O3
Triethanolaminoborate - Names and Identifiers
| Name | orthoboric acid, compound with 2,2',2''-nitrilotriethanol |
| Synonyms | Triethanolaminoborate Triethanolammonium borate boric acid, compounded with triethanolamine Boric acid (H3BO3), compd. with 2,2,2-nitrilotrisethanol orthoboric acid, compound with 2,2',2''-nitrilotriethanol BORIC ACID (H3BO3), COMPOUND WITH 2,2'',2 -NITRILOTRIS(ETHANOL) |
| CAS | 10049-36-2 |
| EINECS | 2331759 |
Triethanolaminoborate - Physico-chemical Properties
| Molecular Formula | C6H15NO3.xBH3O3 |
| Molar Mass | 211.02 |
Triethanolaminoborate - Introduction
orthoboric acid, compound with 2,2 ',2 "-nitrilotriethanol is known as boronic acid tris (2,2',2"-nachine tris [ethanol]) with the chemical formula B(OH)3 · N(CH2CH2OH)3. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
Boric acid tris (2,2 ',2 "-nitrogen tris [ethanol]) is a colorless crystalline solid, soluble in water and alcohol. It is an acidic compound that can react with bases to form salts. The structure of the compound contains functional groups of boric acid and amino alcohol, with similar properties of boric acid and alcohol.
Use:
Boric acid tris (2,2 ',2 "-Nakagawa tris [ethanol]) has some important applications in the field of chemistry. It can be used as a synthesis catalyst for boric acid esters for the esterification of alcohols and ethers. In addition, in organic synthesis, it can also be used as a protective group of hydroxyl phosphate, protecting functional groups with active hydrogen atoms to avoid accidental reactions with other reagents.
Method:
The preparation method of boric acid tris (2,2 ',2 "-nitrogen tris [ethanol]) is relatively simple, and can be obtained by reacting boric acid and 2,2',2"-nitrogen tris [ethanol] in an appropriate solvent. The reaction conditions are generally carried out at room temperature.
Safety Information:
Boric acid tris (2,2 ',2 "-nitrogen chuantri [ethanol]) is relatively safe and non-toxic under normal circumstances. However, as a chemical, you still need to follow some basic operating procedures, such as wearing protective gloves and glasses, and ensuring that you operate in a well-ventilated place. In addition, avoid contact of the compound with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical advice.
Nature:
Boric acid tris (2,2 ',2 "-nitrogen tris [ethanol]) is a colorless crystalline solid, soluble in water and alcohol. It is an acidic compound that can react with bases to form salts. The structure of the compound contains functional groups of boric acid and amino alcohol, with similar properties of boric acid and alcohol.
Use:
Boric acid tris (2,2 ',2 "-Nakagawa tris [ethanol]) has some important applications in the field of chemistry. It can be used as a synthesis catalyst for boric acid esters for the esterification of alcohols and ethers. In addition, in organic synthesis, it can also be used as a protective group of hydroxyl phosphate, protecting functional groups with active hydrogen atoms to avoid accidental reactions with other reagents.
Method:
The preparation method of boric acid tris (2,2 ',2 "-nitrogen tris [ethanol]) is relatively simple, and can be obtained by reacting boric acid and 2,2',2"-nitrogen tris [ethanol] in an appropriate solvent. The reaction conditions are generally carried out at room temperature.
Safety Information:
Boric acid tris (2,2 ',2 "-nitrogen chuantri [ethanol]) is relatively safe and non-toxic under normal circumstances. However, as a chemical, you still need to follow some basic operating procedures, such as wearing protective gloves and glasses, and ensuring that you operate in a well-ventilated place. In addition, avoid contact of the compound with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical advice.
Last Update：2024-04-10 22:29:15
