추천 제품
분석
98%
양식
solid
반응 적합성
reagent type: reductant
mp
124-128 °C (lit.)
작용기
amine
SMILES string
[BH4-].CCCC[N+](CCCC)(CCCC)CCCC
InChI
1S/C16H36N.BH4/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H4/q+1;-1
InChI key
GMBOFJFPOCGSOI-UHFFFAOYSA-N
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일반 설명
Tetrabutylammonium borohydride is used for the reduction of carboxylic acids, aldehydes, and ketones.
애플리케이션
Selective reducing agent for β-ketoamides, β-ketoesters, and carbohydrate derivatives.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B - Water-react 2
Storage Class Code
4.3 - Hazardous materials which set free flammable gases upon contact with water
WGK
WGK 3
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Tetrabutylammonium borohydride
Raber DJ and Guida WC
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Chemistry Letters (Jpn), 1469-1469 (1992)
Tetrahedron, 49, 11169-11169 (1993)
Matthew N McCarroll et al.
Nature communications, 10(1), 4078-4078 (2019-09-11)
Anesthetics are generally associated with sedation, but some anesthetics can also increase brain and motor activity-a phenomenon known as paradoxical excitation. Previous studies have identified GABAA receptors as the primary targets of most anesthetic drugs, but how these compounds produce
Abderrahman Atifi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(53), 13076-13086 (2017-07-26)
The solvent environment around iron porphyrin complexes was examined using mixed molecular/RTIL (room temperature ionic liquid) solutions. The formation of nanodomains in these solutions provides different solvation environments for substrates that could have significant impact on their chemical reactivity. Iron
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