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Amides

Catalog file

The amide anion is the conjugate base of ammonia, NH2-. It is an extremely strong base, due to the extreme weakness of ammonia as a Bronsted acid. Amides undergo many chemical reactions, usually through an attack on the carbonyl breaking the carbonyl double bond and forming a tetrahedral intermediate.

Catalog file

CodeProduct NameUN No.IMCOCAS No.MSDSCOAs
3715P2-ETHOXYBENZAMIDE 97% Extra Pure--938-73-8MSDSCOAs
005144-ACETAMIDOPHENOL 98% Extra Pure--103-90-2MSDSCOAs
027384-CHLOROBENZENESULFONAMIDE 98% Extra pure--98-64-6MSDSCOAs
00510ACETAMIDE 98.5% For Synthesis--60-35-5MSDSCOAs
00520ACETANILIDE 98.5% Extra Pure--103-84-4MSDSCOAs
00529ACETOACETANILIDE 98% For Synthesis--102-01-2MSDSCOAs
01426ANTHRANILAMIDE 99% For Synthesis--88-68-6MSDSCOAs
01800BENZAMIDE 98% For Synthesis--55-21-0MSDSCOAs
01810BENZANILIDE 98% For Synthesis--93-98-1MSDSCOAs
03114CYANOACETAMIDE 98% For Synthesis--107-91-5MSDSCOAs
03320DICYANADIAMIDE 98% Extra Pure--461-58-5MSDSCOAs
00148FORMAMIDE 98% Extra Pure EUC Required--75-12-7MSDSCOAs
00149FORMAMIDE 99.5% AR/ACS EUC Required--75-12-7MSDSCOAs
0150DFORMAMIDE 99% For UV Spectroscopy EUC Required--75-12-7MSDSCOAs
4048DHEXAMETHYLPHOSPHORIC ACID TRIAMIDE 98.5%30829680-31-9MSDSCOAs
04205IODOSUCCINIMIDE 97% For Synthesis--516-12-1MSDSCOAs
04136N-(HYDROXYMETHYL) PHTHALIMIDE 96%NANA118-29-6MSDSCOAs
02185N,O-BIS-(TRIMETHYLSILYL) TRIFLUORO ACETAMIDE 98%29243, 825561-30-2MSDSCOAs
00566N-ACETYLGLYCINAMIDE 96% Extra Pure--2620-63-5MSDSCOAs
6338Dp-TOLUENE SULPHONAMIDE 98% For Synthesis--70-55-3MSDSCOAs
05636SALICYLAMIDE 99% Extra Pure--65-45-2MSDSCOAs
5752DSODAMIDE 95% Extra Pure13904.37782-92-5MSDSCOAs
06174SULPHANILAMIDE 99% Extra Pure--63-74-1MSDSCOAs
06175SULPHANILAMIDE 99% AR--63-74-1MSDSCOAs
06259THIOACETAMIDE 98.5% Extra Pure--62-55-5MSDSCOAs
06260THIOACETAMIDE 99% AR--62-55-5MSDSCOAs

Details

The amide anion is the conjugate base of ammonia, NH2-. It is an extremely strong base, due to the extreme weakness of ammonia as a Bronsted acid. Amides undergo many chemical reactions, usually through an attack on the carbonyl breaking the carbonyl double bond and forming a tetrahedral intermediate.

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