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Available Variants25 g
CHA.19852-25g
Price
€252.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.19852-25g | €252.00 |
97%
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) | C6H11ClO2 |
|---|---|
| CAS Number | 4362-40-7 |
| Molecular Weight | 150.60 |
| NACRES | NA.22 |
| PubChem Substance ID | 24879130 |
| UNSPSC Code | 12352100 |
| EC Number | 224-452-5 |
| MDL number | MFCD00046097 |
| Assay | 97% |
Safety Information Handling visibility
| pictograms |
GHS02
GHS06
  GHS02,GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H226,H301 |
| pcodes | P210 - P233 - P240 - P241 - P242 - P301 + P310 |
| Hazard Classifications | Acute Tox. 3 Oral - Flam. Liq. 3 |
| Storage Class | 3 - Flammable liquids |
| wgk | WGK 3 |
| flash_point_f | 127.9 °F - closed cup |
| flash_point_c | 53.3 °C - closed cup |
| ppe | Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
4-Chloromethyl-2,2-dimethyl-1,3-dioxolane, with the CAS registry number 4362-40-7, is a chemical compound that has been utilized in various organic synthesis reactions. This compound is a dioxolane derivative, featuring a chloromethyl group attached to a 2,2-dimethyl-1,3-dioxolane ring. The presence of the chloromethyl group renders this compound a useful intermediate for the preparation of other organic molecules, including pharmaceuticals and agrochemicals. Its reactivity towards nucleophilic substitution reactions makes it a valuable building block in the construction of complex molecules. Furthermore, the dioxolane ring provides a protected form of a 1,2-diol, which can be deprotected under acidic conditions to reveal the original diol functionality, thus expanding its utility in synthetic chemistry applications. This compound is typically handled with care due to its potential reactivity and toxicity.
