Ordering
Available Variants100 mg
CHA.72493-100mg
Price
€213.60
Available – Dispatch in 14 days
10 g
CHA.72493-10g
Price
€187.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 mg | CHA.72493-100mg | €213.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.72493-10g | €187.80 |
>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
| Empirical Formula (Hill Notation) | C4H8N2O4 |
|---|---|
| CAS Number | 1955-68-6 |
| Molecular Weight | 148.12 |
| UNSPSC Code | 12352209 |
| eCl@ss | 32160406 |
| PubChem Substance ID | 24891095 |
| NACRES | NA.26 |
| MDL number | MFCD00050389 |
Safety Information Handling visibility
| 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
L-Aspartic acid β-hydroxamate, with the CAS number 2909-79-7, is a compound of interest in various biochemical and pharmacological contexts. It is an inhibitor of the enzyme aminopeptidase N, which plays a role in the metabolism of various peptides. The compounds structure is characterized by a hydroxamate group attached to the β-carbon of the L-aspartic acid molecule. L-Aspartic acid β-hydroxamate has been studied for its potential therapeutic applications, including its ability to inhibit the growth of certain types of cancer cells. Additionally, it has been used as a research tool to investigate the biological functions of aminopeptidase N and other related enzymes. Further studies are needed to fully elucidate the mechanisms of action and potential uses of L-Aspartic acid β-hydroxamate in various biological systems. Its biochemical properties make it a valuable compound for ongoing research in the field.
