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Merck
모든 사진(3)

주요 문서

195758

Sigma-Aldrich

Tetramethylammonium bromide

98%

동의어(들):

TMAB

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크기 선택

100 G
₩117,131
500 G
₩146,871

₩117,131


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100 G
₩117,131
500 G
₩146,871

About This Item

Linear Formula:
(CH3)4N(Br)
CAS Number:
Molecular Weight:
154.05
Beilstein:
3620955
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.21
분석:
98%
양식:
solid

₩117,131


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벌크 견적 요청

Quality Level

분석

98%

양식

solid

mp

>300 °C (lit.)

작용기

amine

SMILES string

[Br-].C[N+](C)(C)C

InChI

1S/C4H12N.BrH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1

InChI key

DDFYFBUWEBINLX-UHFFFAOYSA-M

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관련 카테고리

일반 설명

Tetrabutylammonium bromide is a quaternary ammonium compound that is widely used as a phase transfer catalyst.[1] Absolute viscosities of its aqueous solutions have been measured at various temperatures (20,25 and 30°C).[2] Various physical properties (activity coefficient up to saturation, conductance, density and solubility in water) of TMABr have been evaluated.[3]
Tetramethylammonium bromide (TMABr) is a quaternary ammonium salt that is widely used as a phase transfer catalyst.[1] Absolute viscosities of its aqueous solutions have been measured at various temperatures (20,25 and 30°C).[2] Various physical properties (activity coefficient up to saturation, conductance, density and solubility in water) of TMABr have been evaluated.[3] Its impact on the first order rate constant values for the base hydrolysis of the following Fe(II) chelates has been investigated:[4]




  • bis(naphthylidene alanate) (nali)
  • bis(naphthylidene phenylalanate) (nphali)
  • bis(naphthylidene aspartate) (nasi)
  • (naphthylidene histidinate) (nhi)
  • bis(naphthylidenearginate) (nari)

애플리케이션

Tetrabutylammonium bromide may be used in the molten state in the following processes:
  • Synthesis of (2S)-5-(3-phenyl-2-phthalimidylpropanoylamino)isophthalic acid.[5]
  • Synthesis of alkyl-substituted pyrroles in the absence of catalyst and organic solvent.[6]
  • Synthesis of dithioacetals from acetals by transthioacetalisation in a solvent free environment.[7]
  • Synthesis of polyamides (PAs) by the polymerization of terephthalic acid and diisocyanates.[8]
  • Catalyze the addition of thiols to conjugated alkenes.[9]
  • Dehydrochlorination of poly(vinyl chloride). [10]
Tetramethylammonium bromide may be used as a template in the synthesis of small colloidal zeolite Y nanocrystals.[11]

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 2 Oral

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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문서 라이브러리 방문

이미 열람한 고객

Controlling size and yield of zeolite Y nanocrystals using tetramethylammonium bromide.
Holmberg BA, et al.
Microporous and Mesoporous Materials : The Official Journal of the International Zeolite Association, 59(1), 13-28 (2003)
Viscosity of aqueous solutions. III. Tetramethylammonium bromide and the role of the tetraalkylammonium ions.
Nightingale Jr ER.
The Journal of Physical Chemistry, 66(5), 894-897 (1962)
Dehydrochlorination of poly (vinyl chloride) by aqueous sodium hydroxide solution under two-phase conditions.
Kise H.
Journal of Polymer Science, 20(11), 3189-3197 (1982)
Some physical properties of aqueous solutions of tetramethylammonium bromide and tetramethylammonium iodide
Levien BJ.
Australian Journal of Chemistry, 18(8), 1161-1170 (1965)
Kinetic study of the base-catalyzed hydrolysis of novel high-spin hydrophobic Fe(II)-azomethine amino acid chelates: Salt and structure effects on the reactivity
Russian Journal of General Chemistry, 85, 168-172 (2015)

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