In the present work, we report the electrochemical detection of dopamine (DA) by means of cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CA) in the presence of excess ascorbic acid (AA) and uric acid (UA) using pristine palladium nanoparticles decorated graphene modified glassy carbon electrode (G/PdNPs-GCE). G/PdNPs nanocomposite was synthesized by preparing pristine PdNPs from its precursor palladium acetylacetonate, with morpholineborane as the reducing agent and subsequently assembled them on graphene nanosheets. The nanocomposite was characterized by field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), UV-Vis spectrophotometry and Fourier transform infrared spectroscopy (FTIR). CV, DPV and CA determination of DA showed distinct increase in the current with increasing concentration and a wide range of linearity. The catalytic material exhibited ultra selective detection of dopamine with a peak to peak separation of 90 and 149 mV for AA-DA and DA-UA oxidation respectively. The reduced overpotential for simultaneous oxidation of DA, AA and UA in DPV and CV is also a remarkable feature of the catalytic material. More importantly, the modified electrode exhibited clear and distinct peak for DA in CV and DPV even in the presence of 300 and 450 times excess of AA and UA respectively.DA, an electroactive excitatory catecholamine neurotransmitter coexists with AA and UA in the extracellular fluids of central nervous system (CNS) of mammals. 1 It is produced from its precursor L-Dopa by means of decarboxylation, in the adrenal glands and some parts of the brain. 2 It plays an important role in the brain-body coordination, renal, cardiovascular and hormonal systems. 3 Abnormal levels of DA in humans, often leads to serious disorders like Schizophrenia, Parkinson's disease, ADHD and Huntington's disease. 4 It is also involved in drug addiction affecting the dopaminergic pathways. AA on the other hand plays an important role as an antioxidant and is the vital supplement of our diet. Its deficiency causes scurvy and is essentially involved in functions related to immune system and connective tissues. 5 UA is also a natural antioxidant and primary purine metabolite. Its deficiency is associated with hyperuricemia, Parkinson's disease and gout. 6 Many analytical methods such as spectrophotometry, 7 HPLC, 8 ion chromatography 9 and electrochemical methods 10-12 have been developed hitherto, for the determination of DA. Among them, electrochemical detection has been gaining a lot of importance on account of its low cost, rapid response, ease of operation, miniaturization and low sample volume requirements. 13 Additionally, other techniques are expensive, require extensive sample preparation and specialized equipment. The caveat however is that AA and UA coexisting with DA exhibit overlapping oxidation potentials and pronounced fouling on conventional solid electrodes, complicating the electrochemical detection of DA. 14 Moreover, AA is 100-1000 ...