At Dextrose Technologies Pvt. Ltd., we offer Thin Layer Chromatography (TLC) services for rapid, cost-effective qualitative analysis of compounds and mixtures. TLC is ideal for reaction monitoring, quick purity checks, and herbal/phytochemical screening before moving to advanced techniques like HPLC, LCMS, or GCMS. We deliver clear plate documentation and interpretation to support fast decisions in R&D and QC workflows. Qualitative Compound Identification We support qualitative identification using Rf values and spot visualization under appropriate detection conditions, enabling quick comparison against references or known samples (when provided). Reaction Monitoring We monitor chemical reactions and process steps by tracking the appearance/disappearance of spots over time, helping you decide end-point completion and optimize conditions. Purity Checks We perform quick purity checks to detect major impurities or multiple components in a sample, supporting batch comparison and early-stage QC screening. Herbal and Phytochemical Screening We use TLC for preliminary screening of herbal extracts and phytochemical fractions to guide fractionation, method development, or targeted analysis. Deliverables * TLC plate images/documentation * Rf values and observation summary * Interpretation notes aligned to your objective * Optional recommendation for confirmatory HPLC/LCMS/GCMS when needed Get started Share your sample type, solvent system preference (if any), and objective (ID/reaction monitoring/purity/herbal screening). We’ll recommend an efficient TLC workflow.

At Dextrose Technologies Pvt. Ltd., we provide Quality Control (QC) Testing to support batch release, routine compliance, and in-process control. Our chromatography-based QC services deliver consistent, calibration-based results with clear documentation and regulatory-aligned reporting. We help you reduce batch risk, maintain trendable quality metrics, and move faster through internal QA review. Assay Testing (HPLC / RP-HPLC) Accurate content estimation for APIs, intermediates, and formulations using validated/optimized chromatographic methods and standards-based quantification. Related Substances / Impurity Profiling Separation and monitoring of related substances and impurities to support batch comparison, process control, and product quality assessment. Content Uniformity Testing Testing to evaluate dosage consistency across units with structured reporting for easy review and trending. Residual Solvent Analysis (GC-FID / HS-GCMS) Residual solvent quantification using GC-FID or Headspace GCMS, based on target solvent list, matrix, and required limits (ICH Q3C-oriented where applicable). Volatile Impurity Testing Volatile impurity profiling for troubleshooting and routine QC checks using GC techniques suited to your sample type. System Suitability & Routine QC Analysis System suitability testing (SST) and routine batch analysis with documented acceptance checks and clean reporting. Cleaning Validation Sample Analysis HPLC/GC-based analysis of swab/rinse samples for trace residues to support cleaning validation programs (scope-dependent). Outcome you can expect * Batch release readiness with consistent analytical outputs * Ongoing quality monitoring with trend-ready results * Clear, regulatory-aligned reporting for internal QA and client documentation Get started Share your product type, analyte list, specifications/limits, and sample count. We’ll recommend the most efficient QC

At Dextrose Technologies Pvt. Ltd., we provide Thermogravimetric Analysis (TGA) and Derivative Thermogravimetric Analysis (DTG) for thermal and physicochemical characterization of materials. TGA measures weight change vs temperature/time, while DTG highlights rate of mass loss, helping you evaluate moisture/volatile content, thermal stability, decomposition stages, ash/residue, and composition trends in multi-component systems. Thermogravimetric Analysis (TGA) We generate TGA curves to quantify mass loss steps and residual mass under defined heating programs and atmospheres (as per scope). Derivative Thermogravimetric Analysis (DTG) DTG profiles help separate overlapping events and identify key decomposition temperatures by showing the mass-loss rate peaks. Moisture and Volatile Content Determination We quantify early-stage mass loss attributed to moisture and low-boiling volatiles, useful for raw material control and process optimization. Thermal Stability and Decomposition Profiling We assess onset temperatures and decomposition stages to compare batches, evaluate stability, and understand thermal behavior under heating. Ash Content and Residue Analysis We report final residue/ash percentage to support inorganic content assessment and compositional comparison. Composition Analysis of Multi-Component Systems We interpret multi-step mass-loss behavior to provide composition insights (e.g., binder/filler/organic fraction trends), with recommendations for confirmatory techniques if required. Deliverables * TGA and DTG curves with key temperatures (onset/peaks) * % mass loss by stage + final residue/ash % * Comparative summary across samples/batches * Interpretation notes aligned to your objective Get started Share your material type, expected temperature range, sample form, and objective (moisture, stability, ash, composition). We’ll recommend the right TGA/DTG program and reporting format.

At Dextrose Technologies Pvt. Ltd., our R&D Analytical Support helps teams move faster from idea to data with the right analytical strategy and clear, decision-ready reporting. We support method development, compound understanding, reaction tracking, and early impurity/degradation visibility—so you can shorten development cycles and reduce trial-and-error. HPLC / RP-HPLC Method Development & Optimization We develop and optimize chromatography methods (column, mobile phase, gradient, flow, detection) to achieve strong resolution, repeatability, and robustness for your sample type. Assay Method Development for APIs & Formulations Calibration-based assay methods for APIs, intermediates, and formulations with clear reporting units and suitability checks as applicable. LCMS-Based Molecular Weight Confirmation Mass confirmation for non-volatile compounds to support identity verification, batch comparison, and early-stage characterization. Structural Elucidation (Small Molecules) Support for small-molecule structural understanding using MS-based interpretation (scope-dependent), with clear notes and next-step recommendations when needed. Impurity and Degradation Product Identification We profile impurities and degradation products to provide early visibility into risks and to guide method refinement and process decisions. Reaction Monitoring (HPLC / TLC) Fast reaction tracking to support endpoint decisions and process optimization, reported in a structured and easy-to-interpret format. Peptide & Small Molecule LCMS Analysis LCMS analysis for peptides and small molecules (scope-dependent), supporting mass confirmation and profiling. Exploratory Bioanalytical LCMS (Non-GLP) Exploratory analysis for R&D (non-GLP) with workflows tailored to matrix complexity and required sensitivity. Outcome you can expect * Robust analytical methods suitable for R&D progression * Early impurity and degradation visibility * Faster development cycles with clearer decisions Get started Share your compound class, sample matrix, development stage, and goal (method development, impurity ID, reaction monitoring). We’ll propose the fastest, most reliable plan.

At Dextrose Technologies Pvt. Ltd., we provide Gas Chromatography–Mass Spectrometry (GCMS / GC–MS) services for identification and profiling of volatile and semi-volatile compounds in complex samples. GCMS combines strong chromatographic separation with mass spectral confirmation to support unknown peak identification, impurity profiling, and screening studies for R&D and industrial applications. Volatile and Semi-Volatile Compound Identification We identify volatile and semi-volatile compounds using GC separation and MS-based spectral interpretation, supporting troubleshooting, screening, and confirmation workflows. Impurity Profiling We detect and profile impurities and unknown peaks to support batch comparison, contamination investigations, and process optimization. Extractables and Leachables (Screening) We offer screening-level E&L studies to evaluate potential extractable/leachable compounds from packaging, plastics, tubing, or contact materials (scope-dependent, non-regulatory screening unless specified). Flavor and Fragrance Component Analysis We can support fragrance/flavor component analysis only when identification is feasible within our available spectral resources and project scope. (If a dedicated fragrance library is required, we will clarify feasibility upfront.) Environmental and Industrial Sample Analysis We analyze VOC/SVOC profiles in environmental and industrial samples (water/soil/air extracts, process samples, materials) for screening, comparison, and investigation needs. Deliverables * Chromatograms + peak tables * Mass spectra and ID summary for identified peaks (where applicable) * Impurity/profile interpretation notes * Quantification support when standards and reporting limits are defined Get started Share your sample type, target analytes (if known), expected concentration range, and whether you need identification only or identification + quantification.

At Dextrose Technologies Pvt. Ltd., we provide Liquid Chromatography–Mass Spectrometry (LCMS / LC–MS/MS) services for high-confidence molecular weight confirmation, compound identification, and impurity/degradation profiling. LCMS is ideal for non-volatile and thermally sensitive compounds where mass-based confirmation is required. We support R&D and exploratory projects with clear reporting and practical interpretation. Molecular Weight Confirmation We confirm molecular mass and assess molecular ions/adducts (as applicable) to support identity verification and batch comparison. Compound Identification and Characterization We support compound identification using LC separation plus MS/MS-based fragmentation (scope-dependent), enabling stronger confidence than chromatography alone. Impurity Identification and Profiling We detect and profile impurities in complex mixtures and help prioritize unknown peaks for follow-up characterization. Degradation Product Identification We support stability investigations by detecting and identifying degradation products formed under storage or stress conditions (as applicable to your study plan). Metabolite Identification For exploratory studies, we can support metabolite detection/identification workflows based on the sample type and objective (project-dependent). Bioanalytical Sample Analysis (non-GLP exploratory) We handle exploratory bioanalytical analysis for R&D (non-GLP), with method approach finalized based on matrix complexity and target sensitivity. Peptide and Small Molecule Analysis We support peptide and small molecule analysis (project scope dependent), including mass confirmation and profiling. MS Data Interpretation and Reporting We provide structured reports with chromatograms, key ions, observed masses, and interpretation notes—so teams can act quickly. Deliverables * Chromatograms + peak tables * Observed m/z values and spectra/MSMS details (where applicable) * Impurity/degradation profiling summary * Quantitative results (if calibration standards are provided/defined) * Clear conclusions and next-step recommendations Get started Share your sample type, expected mass range, target analytes (if known), and objective (ID/impurities/degradation). We’ll recommend the most reliable LCMS approach.

At Dextrose Technologies Pvt. Ltd., we provide Liquid Chromatography (HPLC / RP-HPLC) services for accurate separation and quantification of compounds in complex matrices. We support both R&D and routine QC with method development, impurity profiling, stability studies, and compliance-focused testing—delivered with clear documentation and decision-ready reports. Method Development and Optimization We develop and optimize HPLC/RP-HPLC methods by selecting suitable columns, mobile phases, gradients, flow, and detection conditions to achieve strong resolution, reproducibility, and robustness for your sample type. Assay Method Development We build assay methods for accurate content estimation of APIs, intermediates, excipients, or key markers, using calibration-based quantification and suitability checks as applicable. Impurity Profiling and Related Substances Analysis We separate and monitor impurities and related substances to support batch comparison, troubleshooting, and product quality assessment. Stability-Indicating Method Development We design methods that can distinguish the main compound from degradation products, supporting stability studies and shelf-life evaluation. Dissolution Sample Analysis We analyze dissolution samples to quantify release profiles and compare formulations or process batches. Content Uniformity Testing We support content uniformity analysis to evaluate dosage consistency across units, reported clearly in a structured format. Degradation and Forced Degradation Studies We perform controlled degradation studies to understand breakdown pathways and to support stability-indicating method development. Cleaning Validation Sample Analysis We analyze swab/rinse samples by HPLC to support cleaning validation programs with sensitive, trace-level quantification (scope-dependent). Deliverables * Chromatograms + peak tables (RT/area/area%) * Quantitative results (%, ppm, mg/mL—based on requirement) * Method conditions and key observations (system suitability notes where applicable) * Summary interpretation with clear conclusions and next-step recommendations Get started Share your analyte list, sample matrix, target limits, and intended use (R&D/QC/validation). We’ll recommend the best HPLC/RP-HPLC workflow and reporting format.

At Dextrose Technologies Pvt. Ltd., we provide antimicrobial susceptibility and efficacy testing to help researchers and product teams evaluate how bacteria and fungi respond to antimicrobial agents. Our testing supports R&D, comparative screening, formulation development, and quality investigations with controlled study conditions, clear documentation, and decision-ready reporting. Antimicrobial Susceptibility Testing (AST) Disc Diffusion Method: Zone-of-inhibition based screening for comparative susceptibility assessment. MIC Determination: Minimum Inhibitory Concentration to identify the lowest concentration that inhibits visible growth. MBC Determination: Minimum Bactericidal Concentration to assess killing endpoints where required. Time-Kill Assays (Kill Curve Studies) We evaluate antimicrobial effect over time by measuring viability at defined timepoints, enabling comparison of efficacy kinetics across agents or concentrations. Antifungal Susceptibility Testing Susceptibility assessment for fungal isolates against antifungal agents, supporting research and screening objectives. Synergistic and Combination Studies We assess combination effects (additive/synergistic/antagonistic trends) to support optimization of multi-agent strategies and formulations. Deliverables Results summary (AST/MIC/MBC/time-kill outputs as applicable) Data tables and interpretation notes aligned to your objective Clear documentation of test conditions and sample identifiers Note: Testing is intended for laboratory, research, and quality purposes. Clinical decisions should be made only by qualified healthcare professionals.

At Dextrose Technologies Pvt. Ltd., we offer Microbial Isolation & Identification services to support research, quality testing, and industrial microbiology. Using sterile, standardized workflows, we isolate microbes from diverse samples, establish pure cultures, apply differential staining, and perform morphology/biochemical-based characterization to generate reliable identification support and clear documentation. Bacterial Isolation and Pure Culture Establishment We perform culture enrichment, streaking, and colony purification to obtain pure bacterial cultures with contamination control and growth documentation. Fungal Isolation and Identification We isolate fungi using appropriate media and incubation conditions, followed by macroscopic and microscopic assessment for identification support. Microbial Staining Techniques We provide staining-based visualization for differentiation and purity checks, including: * Gram staining – Gram reaction and bacterial morphology * Spore staining – endospore detection and differentiation * Acid-fast staining – detection of acid-fast organisms (where applicable) Morphological and Biochemical Characterization We document colony characteristics and microscopic features and perform basic biochemical characterization as per scope, enabling practical classification support for R&D and QC needs. Deliverables * Culture observations (growth pattern, colony morphology) * Staining results with interpretation notes * Microscopy images (where applicable) * Summary report with clear conclusions and next-step recommendations if needed Get started Share your sample type, objective (screening/QC/troubleshooting), and number of samples—we’ll propose the right isolation and identification workflow.