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Available Variants1 mg
CHA.44874-1mg
Price
€455.20
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.44874-1mg | €455.20 |
≥98 atom % 13C, ≥98% (CP)
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) | 13C6C4H9O3N |
|---|---|
| Molecular Weight | 197.14 |
| UNSPSC Code | 12352106 |
| PubChem Substance ID | 329769173 |
| NACRES | NA.12 |
| Isotopic purity | ≥98 atom % 13C |
| Assay | ≥98% (CP) |
| Mass shift | M+6 |
| Form | powder |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
5-Hydroxyindole-3a,4,5,6,7,7a-13C6-3-acetic acid, with the CAS number 54-16-0, is a labeled compound used in various biochemical and pharmacological studies. This isotopically labeled molecule is a derivative of 5-hydroxyindoleacetic acid, a metabolite of serotonin, and is often employed as a standard or internal control in analytical techniques such as mass spectrometry and nuclear magnetic resonance spectroscopy. The incorporation of six 13C atoms into the molecule enables researchers to distinguish it from its naturally occurring counterpart, allowing for accurate quantification and tracing in complex biological systems. As a result, 5-Hydroxyindole-3a,4,5,6,7,7a-13C6-3-acetic acid is a valuable tool in the investigation of serotonin metabolism and related neurological disorders, providing valuable insights into the underlying biochemical processes. Its use facilitates the development of new diagnostic and therapeutic strategies.
