1. Home
  2. »
  3. Solutions

Solutions

Our extensive chemical capabilities cover a variety of complex chemistries and multi-step synthesis making us a competent partner for existing and new molecules.

  • Vapour phase fluorination using AHF
  • Halex reactions using NaF / KF – Established process with high recovery and recycling of the solvent
  •  Reduction
    • Aromatic Ring
    • Double Bond
    • Nitro to Amine
    • Nitrile to Alkyl Amine
    • Dehalogenations
  • Use of precious catalysts like Pd, Pt, Ni, Co, etc with efficient regeneration
  • Carbonyl compounds to corresponding alcohols and alkanes
  • Conversion of aryl methyl group to carboxylic acid using HNO3, NaOCl, H2O2
  • Successful piloting of Grignard reactions taking into account high complexities and safety aspects involved
  • Successful recovery and recycling of solvents
  • Expertise in alkylation and acylation using various metal halide catalyst
  • Expertise in making α,β-unsaturated aromatic acid or α-substituted β-aryl acrylic acid
  • Recycling of the excess salt formation
  • With in-house generated boronic acid
  • Successful recovery and recycling of the precious metal
  • Using Bromine, Aqueous HBr, HBr in acetic acid
  • Capability to recover the bromine from HBr
  • Expertise in O, C and N Alkylations with aliphatic, aromatic and heterocyclic substrates
  • Experience of synthesizing various heterocycles involving reagents like Hydrazine Hydrate, Monomethyl hydrazine and Sulphur compounds
  • Using Carbon monoxide , precious metal catalysts at high temperature  and pressure to introduce carboxylic acid and its derivatives
  • Introduction of aldehyde and ketone group in aromatic ring
  • Expertise in reaction under high temperature (up to 200°C) and pressure (up to 60 bar)
  • Involving sulfuric acid , nitric acid or fuming nitric acid
  • Involving Thiourea, Sodium Poly sulfide and Mercaptans
  • Conversion of halo into cyano group with sodium cyanide
  • Dehydration of carboxamide to nitrile
  • Experience in successfully handling Cyanide waste
  • Experience in reaction to introduce amino group
  • Experience to convert nitrile to imino-ether salt