Ordering
Available Variants0.1 mg
CHA.49450-0.1mg
Price
€730.40
Available – Dispatch in 14 days
25 μg
CHA.49450-25μg
Price
€237.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
0.1 mg | CHA.49450-0.1mg | €730.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 μg | CHA.49450-25μg | €237.60 |
from Prorocentrum concavum, 92-100% (HPLC), powder, protein phosphatase 1 inhibitor
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) | C44H68O13 |
|---|---|
| CAS Number | 78111-17-8 |
| Molecular Weight | 805.00 |
| UNSPSC Code | 12352106 |
| PubChem Substance ID | 24898069 |
| NACRES | NA.77 |
| MDL number | MFCD00083455 |
| Assay | 92-100% (HPLC) |
| Form | powder |
| Quality level | 200 |
Safety Information Handling visibility
| pictograms |
GHS06
 GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H301 + H311 + H331,H315 |
| pcodes | P261 - P264 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 |
| Hazard Classifications | Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Skin Irrit. 2 |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
Technical Overview & Applications Use-case context
Okadaic acid, with the chemical formula C44H68O13 and CAS number 78111-17-8, is a naturally occurring polyketide compound that has been isolated from several marine sponges. It is a potent inhibitor of protein phosphatases, specifically targeting serine/threonine phosphatases, which are essential enzymes involved in various cellular processes. Okadaic acid has been extensively studied for its potential role in tumor promotion and its ability to induce apoptosis in certain cell types. Additionally, it has been used as a tool in research to investigate cellular signaling pathways and the regulation of protein phosphorylation. Due to its high potency and potential toxicity, handling okadaic acid requires proper precautions and safety measures to avoid exposure and minimize risks. Its unique mechanism of action has made it a valuable compound in biomedical research and cellular biology studies.
