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Merck
모든 사진(2)

주요 문서

292788

Sigma-Aldrich

Potassium methoxide

95%

동의어(들):

Potassium methylate

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About This Item

Linear Formula:
CH3OK
CAS Number:
Molecular Weight:
70.13
Beilstein:
3551544
EC Number:
MDL number:
UNSPSC 코드:
12352107
PubChem Substance ID:
NACRES:
NA.22

분석

95%

양식

solid

SMILES string

[K+].C[O-]

InChI

1S/CH3O.K/c1-2;/h1H3;/q-1;+1

InChI key

BDAWXSQJJCIFIK-UHFFFAOYSA-N

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일반 설명

Potassium methoxide is a basic nucleophile used in the dehalogenation of arylhalides.

애플리케이션

Potassium methoxide can be used:
  • As a methoxylating agent for methoxylation of bromo- and mesyloxyalkanes in the presence of an ionic liquid [bmim][BF4].
  • As a catalyst for the synthesis of dimethyl carbonate and methyl formate.
  • As a catalyst for the transesterification of sunflower oil for the production of biodiesel.

픽토그램

FlameCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Self-heat. 1 - Skin Corr. 1B

보충제 위험성

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 2

Flash Point (°F)

51.8 °F - closed cup

Flash Point (°C)

11 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

The effect of Mo(CO)6 as a co-catalyst in the carbonylation of methanol to methyl formate catalyzed by potassium methoxide under CO, syngas and H2 atmospheres. HP-IR observation of the methoxycarbonyl intermediate of Mo(CO)6.
Jali S, et al.
J. Mol. Catal. A: Chem., 348(1-2), 63-69 (2011)
Significantly enhanced reactivities of the nucleophilic substitution reactions in ionic liquid.
Kim DW, et al.
The Journal of Organic Chemistry, 68(11), 4281-4285 (2003)
Synthesis of dimethyl carbonate from methanol and carbon dioxide using potassium methoxide as catalyst under mild conditions.
Cai Q, et al.
Catalysis Letters, 103(3-4), 225-228 (2005)
Integrated biodiesel production: a comparison of different homogeneous catalysts systems.
Vicente G, et al.
Bioresource Technology, 92(3), 297-305 (2004)
E Ballesteros et al.
Journal of chromatography. A, 719(1), 221-227 (1996-01-05)
An automated gas chromatographic method for the simultaneous determination of cholesterol, alpha-tocopherol and alpha-tocopheryl acetate in edible oils and fats without derivatization is reported. Interferences from lipid material are avoided by using a continuous system to transesterify triglycerides with potassium

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