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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
(CH3CH2CH2CH2)4N(OH)
CAS 번호:
Molecular Weight:
259.47
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
3571228
Concentration:
~40% in H2O (~1.5 M)
Form:
liquid
제품 이름
Tetrabutylammonium hydroxide solution, technical, ~40% in H2O (~1.5 M)
InChI
1S/C16H36N.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1
SMILES string
[OH-].CCCC[N+](CCCC)(CCCC)CCCC
InChI key
VDZOOKBUILJEDG-UHFFFAOYSA-M
grade
technical
form
liquid
Quality Level
reaction suitability
core: ammonium
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
concentration
~40% in H2O (~1.5 M)
impurities
≤3% halides (as bromide)
density
0.995 g/cm3
anion traces
sulfate (SO42-): ≤3000 mg/kg
greener alternative category
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General description
The product is ~40% solution of tetrabutylammonium hydroxide in H2O. Tetrabutylammonium hydroxide has been synthesized from tetrabutylammonium iodide. TBAOH dissolved in anhydrous isopropyl alcohol is widely employed as titrant for weak acids.
Application
Tetrabutylammonium hydroxide solution (TBAOH) may be used in the following studies:
- For the dissolution of 10wt% cellulose under room temperature conditions.
- As a catalyst during the synthesis of 1,2,4-oxadiazoles.
- Preparation of TBAOH salts of fatty acids.
Features and Benefits
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Disclaimer
may crystallize; can be redissolved on heating to 40°C
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1
저장 등급
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
B B Y Lau et al.
Bioresource technology, 197, 252-259 (2015-09-08)
Aqueous solutions of tetrabutylphosphonium hydroxide have been evaluated as pretreatment media for rice husks, prior to sulphuric acid hydrolysis or cellulase enzymatic hydrolysis. Varying the water:tetrabutylphosphonium hydroxide ratio varied the rate of delignification, as well as silica, lignin and cellulose
Tetrabutylammonium hydroxide as titrant in nonaqueous media.
Harlow GA, et al.
Analytical Chemistry, 28(5), 787-791 (1956)
Construction of 3, 5-substituted 1, 2, 4-oxadiazole rings triggered by tetrabutylammonium hydroxide: a highly efficient and fluoride-free ring closure reaction of O-acylamidoximes.
Otaka H, et al.
Tetrahedron Letters, 55(5), 979-981 (2014)
Tetrabutylammonium Hydroxide as Titrant for Acids in Nonaqueous Solutions.
Cundiff RH and Markunas PC.
Analytical Chemistry, 28(5), 792-797 (1956)
Foaming and emulsifying properties of fatty acids neutralized by tetrabutylammonium hydroxide.
Fameau AL, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 403, 87-95 (2012)
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