
Methylmercuric chloride | CAS:115-09-3
Methylmercuric chloride
- 名称:甲基氯化汞 | Methylmercuric chloride
- CAS号:115-09-3
- 别名:Methylmercury monochloride; Monomethyl mercury chloride; NSC 19998
- 分子式:CH3ClHg
- 分子量:251.08
- EINESC号:204-064-2
产品描述
物理化学性质
熔点 | 175 ºC* |
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安全数据
没有数据 | 没有数据 |
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SDS
来源 | SDS样本 |
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没有数据 | 没有数据 |
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Study of different parameters affecting the derivatization of acidic herbicides with trimethylsulfonium hydroxide to make them suitable for gas chromatography analysis.C Díez et al.Journal of chromatography. A, 1125(2), 244-253 (2006-06-20)
The Association between the Urinary Excretion of Trimethylselenonium and Trimethylsulfonium in Humans.Bassam Lajin et al.PloS one, 11(11), e0167013-e0167013 (2016-11-22)
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Urea derivatives are highly active catalysts for the base-mediated generation of terminal epoxides from aldehydes and trimethylsulfonium iodide.Sarah A Kavanagh et al.Organic & biomolecular chemistry, 6(8), 1339-1343 (2008-04-04)
Rapid identification of Legionella species from a single colony by gas-liquid chromatography with trimethylsulphonium hydroxide for transesterification.H P Nalik et al.Journal of medical microbiology, 36(6), 371-376 (1992-06-01)
A high-throughput fatty acid profiling screen reveals novel variations in fatty acid biosynthesis in Chlamydomonas reinhardtii and related algae.Erin L Pflaster et al.Eukaryotic cell, 13(11), 1431-1438 (2014-09-23)
Trimethylsulfonium hydroxide as derivatization reagent for the chemical investigation of drying oils in works of art by gas chromatography.Julien Dron et al.Journal of chromatography. A, 1047(1), 111-116 (2004-10-16)
Reaction efficiency of organic alkalis with various classes of lipids during thermally assisted hydrolysis and methylation.Yasuyuki Ishida et al.Journal of chromatography. A, 1216(15), 3296-3299 (2009-02-19)
Reaction of lipids containing hydroxy groups with trimethylsulfonium hydroxide: formation of O-methyl derivatives.K Vosmann et al.Lipids, 31(3), 349-352 (1996-03-01)
Improved identification of mycobacteria by using the microbial identification system in combination with additional trimethylsulfonium hydroxide pyrolysis.K Müller et al.Journal of clinical microbiology, 36(9), 2477-2480 (1998-08-15)
Interferences in the direct quantification of bisphenol S in paper by means of thermochemolysis.Valentina Becerra et al.Journal of chromatography. A, 1275, 70-77 (2013-01-12)
Effects of charge, volume, and surface on binding of inhibitor and substrate moieties to acetylcholinesterase.S G Cohen et al.Journal of medicinal chemistry, 28(9), 1309-1313 (1985-09-01)
Tetrahedron Letters, 35, 2009-2009 (1994)
A new and rapid method for the assay of bacterial fatty acids using high resolution capillary gas chromatography and trimethylsulfonium hydroxide.K D Müller et al.Zentralblatt fur Bakteriologie : international journal of medical microbiology, 274(2), 174-182 (1990-11-01)
A mechanistic analysis of penetration of glyphosate salts across astomatous cuticular membranes.Jörg Schönherr Pest management science, 58(4), 343-351 (2002-04-27)
Synthesis of Dinaphtho[2,3-d:2',3'-d']anthra[1,2-b:5,6-b']dithiophene (DNADT) Derivatives: Effect of Alkyl Chains on Transistor Properties.Takumi Ishida et al.International journal of molecular sciences, 21(7) (2020-04-05)
Use of an injection port for thermochemolysis-gas chromatography/mass spectrometry: rapid profiling of biomaterials.Farzad Shadkami et al.Journal of chromatography. A, 1216(31), 5903-5910 (2009-06-30)
Prebiotic methylation and the evolution of methyl transfer reactions in living cells.T G Waddell et al.Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 30(6), 539-548 (2001-02-24)
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Solvent effects on methyl transfer reactions. 2. The reaction of amines with trimethylsulfonium salts.H Castejon et al.Journal of the American Chemical Society, 123(25), 6092-6097 (2001-06-21)
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Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position.Irina I Popadyuk et al.Steroids, 127, 1-12 (2017-09-10)
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