Petroleum exploration in presalt reservoirs is reaching increasingly deeper carbonate reservoirs, more and more distant from coastline. Therefore, optimization of investments for a safe and profitable production is critical. Each possible concern on geological conditions that would govern fluid composition and that can bring impact in development cost of an accumulation must be taken into account. In some petroleum accumulations, within presalt reservoirs, along southeastern offshore Brazilian basins, H 2 S was found. Although H 2 S concentrations were significantly lower than most of carbonates worldwide, they are enough to be considered in economical evaluations. Therefore, it is important to identify the process that generated H 2 S and to constraint the main variables that govern its occurrence for a more precise evaluation of the "H 2 S risk", take into consideration possible pit falls during well intervention. In this way, H 2 S is precipitated on site as a salt (Ag 2 S) from the gas produced during the long lasting producing tests, shipped to laboratory and the 34 S/ 32 S ratio is measured. The corresponding δ 34 S value is the main tool for identifying H 2 S origin: if it was formed due to organic (BSR, δ 34 S < −10 ‰) or inorganic (TSR, δ 34 S > +10 ‰) sulfate reduction. Results of δ 34 S CDT obtained in H 2 S from presalt reservoirs of the Santos Basin spread between +10 ‰ and +20 ‰ typical of TSR. However, temperatures of the reservoirs are lower than that inferred for development of TSR (T > ≈120 °C) suggesting that H 2 S was generated in deeper intervals with significantly higher temperatures. More accuracy in the interpretation about the origin, and clues on migration pathways and accumulation are obtained integrating geochemical, geological and well data production. This integrated approach gives to the explorationist the best understanding about the "H 2 S risk" in a specific exploratory target. In this work it will be presented a discussion on the methodology for sampling and measuring δ 34 S for identification of H 2 S origin.