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26 results for "derivatisation reagent"

"derivatisation reagent"

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1,1,1,3,3,3-Hexamethyldisilazane : Chlorotrimethylsilane (HMDS + TMCS) (2:1) Silyl-21 silylation reagent, for GC derivatisation

1,1,1,3,3,3-Hexamethyldisilazane : Chlorotrimethylsilane (HMDS + TMCS) (2:1) Silyl-21 silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Silyl-21 reagent will derivatise amides and many secondary amines and hindered hydroxyls that would not be completely derivatised by HMDS alone.

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1,1,1,3,3,3-Hexamethyldisilazane : Chlorotrimethylsilane (HMDS + TMCS) (2:1:10) in pyridine Silyl-2110 silylation reagent, for GC derivatisation

1,1,1,3,3,3-Hexamethyldisilazane : Chlorotrimethylsilane (HMDS + TMCS) (2:1:10) in pyridine Silyl-2110 silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Silyl-2110 reagent will derivatise alcohols, bile acids, phenols, most steroids, sterols, and sugars that would not be completely derivatised by HMDS alone.

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N,O-Bis(trimethylsilyl)acetamide silylation reagent, for GC derivatisation

N,O-Bis(trimethylsilyl)acetamide silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

BSA is a strong silylation reagent that forms very stable TMS derivatives with a large variety of compounds, e.g., non-sterically hindered alcohols, carboxylic acids, phenols, enols, steroids, (biogenic) amines and alkaloids.

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Chlorotrimethylsilane silylation reagent, for GC derivatisation

Chlorotrimethylsilane silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

TMCS is often used as a catalyst with other trimethylsilyl reagents. Without additives it can be used for preparing TMS derivatives of organic acids. Together with methanol it can be used for methylation.

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Dimethyldichlorosilane silylation reagent, for GC derivatisation

Dimethyldichlorosilane silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

DMCS is used to form dimethylsilyl (DMS) derivatives. These derivatives are much more susceptible to hydrolysis than TMS derivatives. Therefore strictly anhydrous conditions during reaction are very important.

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Pentafluorobenzoyl chloride acylation reagent, for GC derivatisation

Pentafluorobenzoyl chloride acylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Pentafluorobenzoyl chloride (PFBC) will react with hydroxyls, primary and secondary amines, amides and thiols.

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1-(Trimethylsilyl)imidazole silylation reagent, for GC derivatisation

1-(Trimethylsilyl)imidazole silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

TSIM is the strongest hydroxyl silylator; reagent of choice for carbohydrates and most steroids (even highly hindered steroids).

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Heptafluorobutyric anhydride (HFAA) acylation reagent, for GC derivatisation

Heptafluorobutyric anhydride (HFAA) acylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Acylation with HFBA can be used for alcohols, phenols, carboxylic acids, amines, amino acids and steroids forming volatile, stable derivatives suited for GC-FID as well as for GC-ECD detection.

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Trifluoroacetic anhydride acylation reagent, for GC derivatisation

Trifluoroacetic anhydride acylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Acylation with fluorinated acid anhydrides can be used for alcohols, phenols, carboxylic acids, amines, amino acids and steroids forming volatile, stable derivatives suited for FID as well as for ECD detection.

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N-Methyl-bis-trifluoroacetamide acylation reagent, for GC derivatisation

N-Methyl-bis-trifluoroacetamide acylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

This derivitisation reagent is recommended for alcohols, primary and secondary amines as well as for thiols under mild, neutral conditions. MBTFA also forms very volatile derivatives with carbohydrates.

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Trimethylsulphonium hydroxide 0.2 M in methanol alkylation reagent, for GC derivatisation

Trimethylsulphonium hydroxide 0.2 M in methanol alkylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Methylation with TMSH is recommended for free acids, chlorophenoxycarboxylic acids, their salts and derivatives as well as for phenols and chlorophenols. Lipids or triglycerides can be converted to the corresponding fatty acid methyl esters (FAMEs) by a simple transesterification.

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N-Methyl-N-trimethylsilylheptafluorobutyramide (MSHFBA) silylation reagent, for GC derivatisation

N-Methyl-N-trimethylsilylheptafluorobutyramide (MSHFBA) silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Silylation reagent with recommended applications: carboxylic acids, alcohols, phenols, primary and secondary amines and amino acids.

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N-Methyl-N-(trimethylsilyl)trifluoroacetamide silylation reagent, for GC derivatisation

N-Methyl-N-(trimethylsilyl)trifluoroacetamide silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Silylation in GC stands for replacement of active hydrogen atoms by a trimethylsilyl group (TMS derivative).

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HMDS (1,1,1,3,3,3-hexamethyldisilazane) silylation reagent, for GC derivatisation

HMDS (1,1,1,3,3,3-hexamethyldisilazane) silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

HMDS is weak TMS donor. If used as sole reagent, it is slow and not very effective. After addition of catalytic quantities (e.g., 1 %) of TMCS or as a mixture with TMCS it is a fast and quantitative reagent for trimethylsilylation of organic compounds.

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N-Methyl-bis-heptafluorobutyramide (MBHFBA) acylation reagent, for GC derivatisation

N-Methyl-bis-heptafluorobutyramide (MBHFBA) acylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

Acylation with fluorinated bisacylamides is recommended for alcohols, primary and secondary amines as well as for thiols under mild, neutral conditions.

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N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) silylation reagent, for GC derivatisation

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) silylation reagent, for GC derivatisation

Supplier: MACHEREY-NAGEL

MBDSTFA is a silylation reagent that donates a tert-butyldimethylsilyl group (TBDMS) for derivatizing active hydrogen atoms in hydroxyl, carboxyl and thiol groups, primary and secondary amines as well as amino acids. Fast reactions (typically 5–20 min) with high yields (> 96 %). By-products are neutral and volatile.

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