Anthelmintics

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

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

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

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

Fenthion oxon sulfone-( S - methyl -d 3 ) is a deuterated isotope analog of fenthion oxon sulfone-( S - methyl ), a derivative of organophosphorus insecticide fenthion, wherein S -methyl protons are replaced by deuterium. Application

Fenthion-sulfone is one of the metabolites of fenthion which is classified under the organophosphorus group of pesticides. Application Fenthion-sulfone may be used as an analytical reference standard for the determination of fenthion-sulfone in:

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034 . This CRM is traceable to primary material from an NMI, e.

Ferulamide.

Cell Line Origin Fish Fat Head minnow Cell Line Description Derived from tissue posterior to the anus of normal adult minnows. Reported to be capable of growth over a wide temperature range from 4°C-36°C with maximum growth at 34°C.

Fish oil is derived from the tissues of oily fish. It lowers blood pressure and high triglyceride levels.

Fish oil is derived from the tissues of oily fish. It lowers blood pressure and high triglyceride levels.

Flazasulfuron may generally be used as a sulfonylurea herbicide , which is having broad spectrum applications in weed control management. Its mode of action involves the inhibition of branched-chain amino acids, via binding irreversibly to to