
Agrochemicals
Physical and chemical properties of technical grade and various pesticide formulations include:
Active ingredient content (including method development and validation), an overview of various properties of a substance, including color, odor, physical state, UV-VIS absorption spectra, melting and boiling points, water solubility, dissociation constants, hydrolysis, partition coefficient, vapor pressure, relative density, storage stability, flammability, flash point, pH, moisture content, loss on drying, oxidation/reduction, corrosion, aqueous direct photolysis, surface tension, and oxidizing properties, self-ignition, oxidizing properties, flamability, acidity/alkalinity/pH, density, density, specific gravity, flowability, packaging stability, suspensibility, persistent foam, emulsion properties, wettability, degree of dispersion, corrosivity, viscosity, surface tension, and dilution stability.
Storage stability studies
(Accelerated, Long-term term and Multi-location) and Low temperature stability.
The five batch analysis studies follow the linear path listed below:
Pre-screening of 5 batches for impurities, including 3D screening
- Impurity identification and structure elucidation in consultation with the sponsor
- Isolation/synthesis of impurities required for 5-batch analysis
- GLP analysis of 5 batches using validated analytical methods for active ingredient content and impurities
- Characterization of 5 commercial batches along with reference standards by UV, IR, NMR, LC-MS/MS and/or GC-MS as applicable.
Residue and Persistence studies
- Method Development and Validation in diversified matrices
- Residues in Soil
- Residues in Water
- Residues in Plant
- Residue in crops for multiple occasions and multiple locations
- Persistence studies in plant (field), soil (field and lab) and water (lab)
Environmental Fate Studies
- Soil physico analysis
- Activated Sludge/Microbial Activity
- Soil, Plant and Animal Metabolism
- Soil Adsorption and Desorption
- Hydrolysis and Photolysis
- Leaching
- Carbon and Nitrogen Transformation
- Confined Rotation
- Ready Biodegradability
Container compatibility and transport worthiness of packaging materials: Studies
Reactivity with packing material) Studies pesticide technical grade and various pesticide formulations.
Analytical Test Report
A.I. Content and its related impurities and physical and chemical parameters for pesticide technical and formulations.
Biostimulants
- Humic acid and Fulvic acid
- Amino acid (Nitrogenous substances)
- Algae extracts
- Plant extract
- Micro Organisms
- Seaweed extract
- Vitamin extraction
Analysis of Curcuminoids
Curcumin, Dimethoxycurcumin and Bis dimethoxycurcumin
Botanical extracts, including seaweed extracts
Carrageenan content in Sea weed extract, Minerals, total phenolics, Plant hormones:
Auxins, Cytokinins, Gibberellic acid
Amino acids Analysis
Alanine, Arginine, Asparagine, Aspartic Acid, Cysteine, Glutamic acid, Glutamine, Glycine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Proline, Serine, Threonine, Tryptophan, Tyrosine, Valine.
Vitamin Analysis
Coenzyme, Q10 (CoQ10), Vitamin A, Vitamin B1(thiamine), Vitamin B2 (riboflavin), Vitamin B3 (niacin), Vitamin B5 (pantothenic acid), Vitamin B6(pyridoxine, pyridoxal, pyridoxamine), Vitamin B8 (H-biotin),Vitamin B9 (folate)Vitamin C (Ascorbic acid), Vitamin D,Vitamin E (a-
Tocopherol), Vitamin K K1, (Phylloquinone) and K2 (menaquinone)
Nano pesticide formulation synthesis and characterization
Nanoemulsions, Nanoencapsulation, Particle Size and Distribution, Electron Microscopy (TEM/SEM), X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR)
Pharmaceuticals
Nitrosamines Analysis
Nitrosamines are a group of chemical compounds that have attracted significant attention in recent years—not only because of their potential carcinogenicity, but also due to the analytical challenges involved in detecting them at trace levels. Here are some key insights into the field of nitrosamines analysis:
Quantification of NDMA, NDEA, NDPA, NDBA, NPIP, NPYR and NMOR.
Active Pharmaceutical Ingredients (API) and Related Impurities, Genotoxic Impurities & Residual Solvents Testing
Meet Regulatory Standards – Comply with ICH Q3C and USP <467> impurity testing guidelines.
Method development, Analytical method validations, Cleaning Method Validations and Method transfers.
API and formulation drug products
Extra other services for pharma products
QC Testing for Batch Release, Raw Material & Excipient Qualification, Reference Standard Characterization, Solid State Characterization by XRD, Stability and Release Testing, Forced Degradation Stress Testing, Elemental Analysis.