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Available Variants1 mg
CHA.42634-1mg
Price
€289.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
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Available – Dispatch in 14 days
Global Network - International delivery
|
1 mg | CHA.42634-1mg | €289.60 |
chitinase substrate; lysozyme substrate, ≥98% (TLC), powder
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) | C30H44N4O18 |
|---|---|
| CAS Number | 7699-38-9 |
| Molecular Weight | 748.69 |
| UNSPSC Code | 12352204 |
| PubChem Substance ID | 24897686 |
| NACRES | NA.32 |
| MDL number | MFCD00057914 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
4-Nitrophenyl β-D-N,N′,N′′-triacetylchitotriose, with the CAS registry number 7699-38-9, is a synthetic compound derived from chitotriose, a trisaccharide composed of three glucose units. This molecule has been modified with a 4-nitrophenyl group and acetylated at the nitrogen atoms, resulting in a compound with unique chemical and biological properties. The presence of the 4-nitrophenyl group allows for easy detection and quantification, making it a useful tool in biochemical assays. Additionally, the acetylation of the nitrogen atoms enhances the compounds stability and solubility, facilitating its use in various applications, including enzymatic studies and carbohydrate research. The compounds structure and properties make it a valuable reagent in the field of glycoscience, enabling researchers to investigate the biological functions and interactions of chitin and its derivatives.
