N-Methyl-N-(trimethylsilyl)trifluoroacetamide with 1% trimethylchlorosilane

• Catalog No.: 69478
• CAS Number: 24589-78-4
• M. F.: C6H12F3NOSi
• M. W.: 199.2462896

SYNONYMS

• Title: 含 1% 三甲基氯硅烷的 N-甲基-N-(三甲基硅烷基)三氟乙酰胺
• IUPAC name: 2,2,2-trifluoro-N-methyl-N-(trimethylsilyl)acetamide
• IUPAC Traditional name: 2,2,2-trifluoro-N-methyl-N-(trimethylsilyl)acetamide

DATABASE IDS

• PubChem SID: 24885931
• CAS Number: 24589-78-4
• MDL Number: MFCD00000411
• Beilstein Number: 1941550

PROPERTIES

• Empirical Formula (Hill Notation): C6H12F3NOSi
• Grade: for GC derivatization
• Grade: for derivatization
• Flash Point: 26 °C
• Flash Point: 78.8 °F
• Refractive Index: n20/D 1.378
• GHS Signal Word: Warning
• GHS Hazard statements: H226-H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P261-P305 + P351 + P338
• RID/ADR: UN 1993 3/PG 3
• Risk Statements: 10-36/37/38
• Safety Statements: 26
• Hazard Class: 3
• UN Number: 1993
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Application
Addition of Trimethylchlorosilane aids in the derivatization of amides, secondary amines and hindered hydroxy groups. Most volatile of the TMS derivatives often elutes at the solvent front of the GC.

Description (简体中文)

Application
Addition of Trimethylchlorosilane aids in the derivatization of amides, secondary amines and hindered hydroxy groups. Most volatile of the TMS derivatives often elutes at the solvent front of the GC.