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The campaign comprised 27 experiments simulating a range of urban chemical environments, including single-source oxidation experiments (volatile chemical products, cooking, gasoline, and diesel exhaust) and multi-source mixtures representative of present-day Los Angeles, diesel-dominated European cities, and future low-vehicle-emission scenarios, under diverse daytime and nighttime oxidant regimes.\r\nMeasurements include: gas-phase VOCs and oxygenated VOCs by NH4⁺ and H3O⁺ chemical ionisation mass spectrometry (VOCUS and FUSION PTR-TOF); non-methane hydrocarbons (C2–C12) by online GC–MS/FID (GC-ACTRIS and GC-1); trace inorganic gases including NOx, NOy, O3, and HONO by chemiluminescence, UV absorption, and iterative cavity-enhanced DOAS (ICAD); OH, HO2, and RO2 radical concentrations by laser-induced fluorescence (ROxLIF); NO3 radical chemistry by chemical ionisation; total OH reactivity by laser-flash photolysis LIF; aerosol chemical composition by high-resolution aerosol mass spectrometry (AMS), Orbitrap mass spectrometry, WALL-E Orbitrap, and Extractive Electrospray Ionisation (EESI); aerosol volatility and molecular composition by a Filter Inlet for Gases and AEROsols (FIGAERO) coupled to iodide chemical ionisation and by a CHARON inlet coupled to NH4⁺ and H3O⁺ chemical ionisation mass spectrometry; gas-phase molecular composition by a Multi-Reagent Chemical Ionisation Mass Spectrometer (MR-CIMS) operated with iodide, acetone, bromide, and benzene reagent ions; oxygenated compounds by a high-resolution amine time-of-flight instrument (amine-HTOF); aerosol size distributions by Scanning Mobility Particle Sizers (SMPS) and an Electrical Low Pressure Impactor (ELPI); and photolysis frequencies by CCD spectroradiometry. 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