Ordering
Available Variants100 g
CHA.62585-100g
Price
€38.08
Available – Dispatch in 14 days
500 g
CHA.62585-500g
Price
€148.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.62585-100g | €38.08 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 g | CHA.62585-500g | €148.80 |
98%
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
| Linear Formula | (CH3)2CBrCOBr |
|---|---|
| CAS Number | 20769-85-1 |
| Molecular Weight | 229.90 |
| UNSPSC Code | 12352100 |
| NACRES | NA.22 |
| PubChem Substance ID | 24855196 |
| EC Number | 244-017-3 |
| Beilstein/REAXYS Number | 1746128 |
| MDL number | MFCD00000122 |
| Assay | 98% |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405 |
| Hazard Classifications | Eye Dam. 1 - Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | >230.0 °F |
| flash_point_c | > 110 °C |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
α-Bromoisobutyryl bromide, with the CAS number 20769-85-1, is a chemical compound that has been utilized in various organic synthesis reactions. This compound is a brominated derivative of isobutyryl bromide and exhibits reactivity due to the presence of the bromine atoms. α-Bromoisobutyryl bromide is often employed as an initiator or intermediate in the synthesis of complex molecules, including polymers and pharmaceuticals. Its chemical structure consists of a central carbon atom bonded to two bromine atoms, a methyl group, and a carbonyl group, which contributes to its reactivity. The compound is typically handled with caution due to its potential to cause skin and eye irritation, and its use is often carried out in controlled laboratory settings with proper safety protocols in place to minimize exposure risks.
