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Cyclic Imides

A cyclic imide is an imide, consisting of two acyl groups bound to nitrogen, in which the two carbonyl carbons are connected by a carbon chain. Cyclic imide derivatives exhibit potential hypoglycemic, anti-hyperlipidemic, anti-inflammatory, analgesic, and cytotoxic activities, as well as COX-1/COX-2 inhibition, and are agents related to DNA binding and apoptosis induction. Cyclic imides are used in metal-ligand coordinations due to their electron-poor properties.

Product #

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Description

Molecular Formula

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553603 2,3-Dibromomaleimide 97% C4HBr2NO2
129585 Maleimide 99% C4H3NO2
595934 2,3-Dibromo-N-methylmaleimide 99% C5H3Br2NO2
389412 N-Methylmaleimide 97% C5H5NO2
325384 N-Methylsuccinimide 99% C5H7NO2
64940 N-Methoxycarbonylmaleimide ≥97.0% (N) C6H5NO4
773263 N-(2-Hydroxyethyl)maleimide 97% C6H7NO3
444073 N-(2-Hydroxyethyl)succinimide 95% C6H9NO3
63285 N-Maleoyl-β-alanine ≥98.0% (HPLC) C7H7NO4
394815 N-Maleoyl-β-alanine 97% Green Alternative C7H7NO4
562807 N-Propylmaleimide 95% C7H9NO2
41314 2-Maleimidoethyl mesylate technical, ≥90.0% (HPLC) C7H9NO5S
163503 α,α-Dimethyl-β-methylsuccinimide 99% C7H11NO2
135550 3,4,5,6-Tetrachlorophthalimide 97% C8HCl4NO2
422665 4,5-Dichlorophthalimide 97% C8H3Cl2NO2
260908 N-Bromophthalimide 95% C8H4BrNO2
528218 N-Chlorophthalimide 96% C8H4ClNO2
79790 Phthalimide potassium salt purum, ≥99.0% (NT) C8H4KNO2
160385 Phthalimide potassium salt 98% C8H4KNO2
79780 Phthalimide puriss., ≥99.0% (T) C8H5NO2
240230 Phthalimide ≥99% C8H5NO2
524794 3-Aminophthalimide 97% C8H6N2O2
T14206 cis-1,2,3,6-Tetrahydrophthalimide 96% C8H9NO2
386421 N-tert-Butylmaleimide 97% C8H11NO2
559504 N-Methyl-4,5,6,7-tetrafluorophthalimide 97% C9H3F4NO2
252611 N-(Bromomethyl)phthalimide 97% C9H6BrNO2
232424 N-(Chloromethyl)phthalimide 97% C9H6ClNO2
407992 N-Methylphthalimide 98% C9H7NO2
H41803 N-(Hydroxymethyl)phthalimide 97% C9H7NO3
247715 4-Amino-N-methylphthalimide 97% C9H8N2O2
518662 N-Hydroxymethyl-3,4,5,6-tetrahydrophthalimide 98% C9H11NO3
P73005 Pyromellitic diimide 97% C10H4N2O4
556297 2,3-Dichloro-N-phenylmaleimide C10H5Cl2NO2
775207   N-(4-Bromophenyl)maleimide 97% C10H6BrNO2
775215   N-(4-Chlorophenyl)maleimide 97% C10H6ClNO2
78795 N-Phenylmaleimide ≥98.0% (HPLC) C10H7NO2
P27100 N-Phenylmaleimide 97% C10H7NO2
454842 N-Acetylphthalimide 97% C10H7NO3
B66302 N-(2-Bromoethyl)phthalimide 95% C10H8BrNO2
349658 N-(2-Chloroethyl)phthalimide ≥98% C10H8ClNO2
138339 N-(2-Hydroxyethyl)phthalimide 99% C10H9NO3
381543 N-Cyclohexylmaleimide 97% C10H13NO2
557781 N-Benzyl-2,3-dibromomaleimide 97% C11H7Br2NO2
408018 N-Benzylmaleimide 99% C11H9NO2
C5459 N-Carbethoxyphthalimide 96% C11H9NO4
B80003 N-(3-Bromopropyl)phthalimide 98% C11H10BrNO2
358657 3-Maleimidopropionic acid N-hydroxysuccinimide ester 99% C11H10N2O6
860581 α-Methyl-α-phenylsuccinimide 99% C11H11NO2
103063 N-(3-Hydroxypropyl)phthalimide 95% C11H11NO3
N1658 1,8-Naphthalimide 99% C12H7NO2
663034 N-(2-Butynyl)phthalimide 97% C12H9NO2
630861 N-(3-Butynyl)phthalimide 97% C12H9NO2
40923 p-Formylbenzoic acid N-hydroxysuccinimide ester ≥97.0% (HPLC) C12H9NO5
CDS010400 (R)-2-phthalimido-3-buten-1-ol AldrichCPR C12H11NO3
100919 N-(4-Bromobutyl)phthalimide 98% C12H12BrNO2
730424 N-Butylphthalimide 97% C12H13NO2
46124 tert-Butyl N-succinimidyl N,N′-ethylenedicarbamate ≥97.0% C12H19N3O6
663026 N-(2-Pentynyl)phthalimide 97% C13H11NO2
646938 N-(4-Pentynyl)phthalimide 97% C13H11NO2
149241 N-(tert-Butoxycarbonyloxy)phthalimide 97% C13H13NO5
416274 N-Phenylphthalimide 98% C14H9NO2
543993 N-(5-Hexynyl)phthalimide ≥95% C14H13NO2
699519 N-[3-(Trimethylsilyl)-2-propynyl]phthalimide 97% C14H15NO2Si
568600 6-Maleimidohexanoic acid N-hydroxysuccinimide ester 98% C14H16N2O6
P40204 Phthalimidoacetaldehyde diethyl acetal 99% C14H17NO4
437123 N-(tert-Butyldimethylsilyl)phthalimide 99% C14H19NO2Si
404756 N-Benzylphthalimide 99% C15H11NO2
M9775 4-(N-Maleimido)benzophenone C17H11NO3
CDS003969 2,2′-ethylenebis-(4,5,6,7-tetrabromophthalimide) AldrichCPR C18H4Br8N2O4
P7908 N-(1-Pyrenyl)maleimide C20H11NO2
P1913   Polymaleimide mol wt 10,000-20,000