Ordering
Available Variants10 mg
CHA.63411-10mg
Price
€94.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 mg | CHA.63411-10mg | €94.80 |
(E) and (Z) isomers (50:50), analytical standard
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) | C26H29NO2 |
|---|---|
| CAS Number | 68392-35-8 |
| Molecular Weight | 387.51 |
| NACRES | NA.24 |
| UNSPSC Code | 41116107 |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
  GHS08,GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 + H312 + H332,H315,H319,H361fd |
| pcodes | P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338 - P308 + P313 |
| Hazard Classifications | Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
4-Hydroxytamoxifen, with a CAS number of 68047-06-3, is a metabolite of the selective estrogen receptor modulator tamoxifen. It is primarily formed through the hepatic metabolism of tamoxifen, where it is converted by the enzyme cytochrome P450 2D6. As a result, 4-hydroxytamoxifen exhibits a higher affinity for estrogen receptors compared to its parent compound, thereby contributing to the therapeutic efficacy of tamoxifen in the treatment of hormone receptor-positive breast cancer. The compounds ability to bind to estrogen receptors allows it to act as an antagonist, inhibiting the growth-promoting effects of estrogen on cancer cells. This metabolite plays a crucial role in the pharmacological activity of tamoxifen, and its formation is a key factor in determining the drugs overall effectiveness in patients. Its study has contributed significantly to the understanding of tamoxifens mechanism of action.
