17596-96-2

Basic information

• Product Name: TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE
• Synonyms: TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE;bis(trimethylsilyl)lactate;2-(Trimethylsiloxy)propanoic acid trimethylsilyl ester;O,O-BIS(TRIMETHYLSILYL) LACTATE
• CAS NO: 17596-96-2
• Molecular Formula: C₉H₂₂O₃Si₂
• Molecular Weight: 250.43958
• Mol File: 17596-96-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 200°C
• Appearance: /
• Refractive Index: 1.4053
• CAS DataBase Reference: TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE(17596-96-2)
• EPA Substance Registry System: TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE(17596-96-2)

Safety Data

• Hazardous Substances Data: 17596-96-2(Hazardous Substances Data)

Usage

General Description

TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE is a chemical compound that is commonly used as a crosslinking agent and coating material in various industrial applications. It is a derivative of lactic acid and contains trimethylsilyl groups, which make it highly stable and resistant to degradation. TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE is often used in the production of specialty polymers, adhesives, and coatings due to its ability to improve the mechanical and thermal properties of the final products. Additionally, TRIMETHYLSILYL TRIMETHYLSILOXY LACTATE can also act as a lubricant and anti-adhesive agent in certain manufacturing processes, making it a versatile and valuable chemical in the industry.

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 849585-22-4 LACTIC ACID 
• 21149-38-2 2,2,2-trifluoro-N,N-bis(trimethylsilyl)-acetamide 
• 77287-34-4 formamide 
• 25561-30-2 N,O-bis(trimethylsilyl)trifluoroacetamide 

Relevant articles and documents

Silica Metal Oxide Vesicles Catalyze Comprehensive Prebiotic Chemistry

It has recently been demonstrated that mineral self-assembled structures catalyzing prebiotic chemical reactions may form in natural waters derived from serpentinization, a geological process widespread in the early stages of Earth-like planets. We have s

Diastereoselective synthesis and structural determination of 1,3-dioxolan-4-ones from lactic acid and carbonyl derivatives

New 1,3-dioxolan-4-ones were prepared by reacting lactic acid with the corresponding ketones.Depending on steric interactions and the cyclization method chosen, a good selectivity was achieved favoring cis or trans diastereomers.Relative stereochemistry and product conformation is discussed on the basis of NMR spectra.Key Words: dioxolanes / chirality transfer / lactic acid / relative stereochemistry

Analysis of the venom of the Sydney funnel-web spider, Atrax robustus using gas chromatography mass spectrometry

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