Ordering
Available Variants25 g
CHA.69857-25g
Price
€31.12
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.69857-25g | €31.12 |
≥99.0% (AT)
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) | C4H7NOS · HCl |
|---|---|
| CAS Number | 6038-19-3 |
| Molecular Weight | 153.63 |
| NACRES | NA.22 |
| PubChem Substance ID | 57651419 |
| eCl@ss | 42021308 |
| UNSPSC Code | 12352100 |
| EC Number | 227-923-3 |
| MDL number | MFCD00012724 |
| Beilstein/REAXYS Number | 3689338 |
| Assay | ≥99.0% (AT) |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319 |
| pcodes | P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
DL-Homocysteine thiolactone hydrochloride, with the CAS number 6038-19-3, is a chemical compound that plays a significant role in various biochemical processes. It is a thiolactone derivative of the amino acid homocysteine, which is an intermediate in the metabolism of methionine and cysteine. The compound has been studied for its potential implications in cardiovascular disease, as elevated levels of homocysteine have been linked to increased risk of atherosclerosis and thrombosis. DL-Homocysteine thiolactone hydrochloride is also used as a research tool in the study of protein modification and enzymatic reactions, allowing scientists to investigate the mechanisms of homocysteine-induced changes in protein structure and function. Its hydrochloride salt form enhances stability and solubility, making it a convenient reagent for laboratory applications.
