Tris-saturated Phenol

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

4-Octylphenol

4-Octylphenol

Application 4-Phenoxyphenylboronic acid can be used as a reactant: In the Suzuki-Miyaura coupling reaction to synthesize aryl derivatives via C-C bond formation by reacting with different aryl halides over a palladium catalyst. To prepare

4- tert -Octylphenol is a potential environmental pollutant and it exhibits toxic and estrogenic effects on mammalian cells . It binds to estrogen receptors and exerts estrogenic actions in vitro .

4- tert -Octylphenol is a potential environmental pollutant and it exhibits toxic and estrogenic effects on mammalian cells . It binds to estrogen receptors and exerts estrogenic actions in vitro .

4- tert -Octylphenols are classified under the alkylphenol family of compounds. Application 4- tert -Octylphenol may be used as an analytical reference standard for the determination of the analyte in: Human biological samples and water samples by

Application 5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing &#948-valerolactones.

Application 5-Hexenoic acid may be used for the preparation of iodolactone derivatives and fluorine-containing &#948-valerolactones.

Bisphenol A ethoxylate