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N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) per sintesi, Sigma-Aldrich®

Fornitore: Merck

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) per sintesi, Sigma-Aldrich®

MSDS

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide with 1% tert-butylchlorodimethylsilane ≥95.0% (by GC), LiChropur™ for GC derivatisation, Supelco®

Fornitore: Merck

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide with 1% tert-butylchlorodimethylsilane ≥95.0% (by GC), LiChropur™ for GC derivatisation, Supelco®

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) ≥95.0% (by GC)

Fornitore: TCI EUROPE

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) ≥95.0% (by GC)

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) 98%

Fornitore: Thermo Scientific

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) 98%

MSDS

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) 97%

Fornitore: Apollo Scientific

Descrizione: GC derivatising agent for silylation of hydroxy, carboxy, thio & primary and secondary amines.

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) ≥97%

Fornitore: Thermo Scientific

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA) ≥97%

MSDS Certificati

N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA)

Codice catalogo: (HYPETS-48920)

Fornitore: Thermo Fisher Scientific

Codice articolo fornitore: TS-48920

Codice articolo locale: HYPETS-48920

Descrizione: N-(tert-Butyldimethylsilyl)-N-methyltrifluoroacetamide (MTBSTFA)

UOM: 1 * 5 mL

Promo

Non disponibile confezione

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

Codice catalogo: (MANA701440.101)

Fornitore: MACHEREY-NAGEL

Codice articolo fornitore: 701440.101

Codice articolo locale: MANA701440.101

Descrizione: 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.

UOM: 1 * 1 KIT

Promo