Ammonium/bromodiphenhydramine/menthol/potassium

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the

10-Bromodecanoic acid can be prepared from 10-bromodecanol via oxidation.10-Bromodecanoic acid may be employed as an alkylcarboxylate chain source in the preparation of alkylcarboxylate-grafted polyethylenimine.[1] It may also be used in the

100% #2 Diesel Fuel -20mL

CAS No.: 2432-99-7 Solubility: 2 g/l (20°C) Melting Point: >185°C Molar Mass: 201.3 g/mol Bulk Density: 500 kg/m3

11-Bromoundecanoic acid reacts with potassium salt of dimethyl hydantoin to yield 4,4-dimethyl hydantoin-undecanoic acid . Application 11-Bromoundecanoic acid was used in the synthesis of 11-phenoxyundecyl phosphate and 11-hydroxytetradecanoic acid

15(R)-HEDE is isolated by the chromatographic resolution of (&plusmn)15-HEDE. There are no reports of biological activity associated with 15(R)-HEDE in the literature.

15(R)-HEDE is isolated by the chromatographic resolution of (&plusmn)15-HEDE. There are no reports of biological activity associated with 15(R)-HEDE in the literature.

15(R)-HEDE is isolated by the chromatographic resolution of (&plusmn)15-HEDE. There are no reports of biological activity associated with 15(R)-HEDE in the literature.

15(R)-HEDE is isolated by the chromatographic resolution of (&plusmn)15-HEDE. There are no reports of biological activity associated with 15(R)-HEDE in the literature.