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Available Variants1 g
CHA.82811-1g
Price
€154.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.82811-1g | €154.80 |
96%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C6H12O5 |
|---|---|
| CAS Number | 18370-95-1 |
| Molecular Weight | 164.16 |
| NACRES | NA.22 |
| PubChem Substance ID | 329765252 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD09701200 |
| Assay | 96% |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H319 |
| pcodes | P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 |
| Storage Class | 10 - Combustible liquids |
| wgk | WGK 3 |
| flash_point_f | 180.0 °F |
| flash_point_c | 82.2 °C |
Technical Overview & Applications Use-case context
Methyl trimethoxyacetate, with the CAS number 18370-95-1, is a chemical compound that has been utilized in various applications due to its unique properties. It is an ester derivative, specifically a trimethoxyacetic acid ester, which exhibits distinct reactivity and stability characteristics. This compound has been employed as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, where its methoxy groups can participate in further reactions to form complex molecules. The trimethoxy functionality also imparts specific solubility and volatility properties, making methyl trimethoxyacetate a useful reagent in various chemical transformations, including those involving acid or base catalysis, and its handling and storage require standard laboratory precautions to ensure safety and prevent degradation or contamination. Its molecular structure and reactivity profile make it a valuable building block in organic synthesis.
