Purity, engineered at scale.
High purity laboratory chemicals, solvents and excipients trusted by India's leading pharmaceutical manufacturers.
25+ years of expertise. Accountability in every batch.
Our solvents and reagents are backed by application-focused R&D, manufacturing controls that adhere to GMP guidelines and traceability down to the raw materials used.
Customers
25+ Years of Manufacturing
Products Across Grades
Certified
R&D guided by your application
Our development process starts with how a reagent will be used. We focus on the specifications and impurities that matter to its performance in your laboratory.
Controls that follow GMP guidelines
Our controls adhere to GMP guidelines across raw material handling, production, testing and batch release. Quality is part of the manufacturing process at every stage.
Every batch traced to its source
Every product and every batch can be traced back to the raw materials used to manufacture it. This gives your quality team a clear trail to support documentation, investigations and audits.
Expertise behind every product
Work directly with the people who understand the chemistry. Our technical team supports product selection, specification queries and custom requirements, with access to our manufacturing and quality teams.
From LR to LCMS, one standard.
HPLC / LCMS / GCPharma-Grade Solvents
High-purity solvents with controlled UV cutoff, low residue and tight water content, supplied from retail packs to drums.
View catalogue
IP / BP / USP / EPPharmaceutical Excipients
Multi-compendial excipients produced under documented quality controls, supported by full documentation for regulatory filings.
View catalogue
LR / AR / GR / ACSLaboratory Chemicals
Analytical and general reagents manufactured and packed to published specifications, with a certificate of analysis for every batch.
View catalogueAI-native manufacturing
Every batch we make
teaches the next one.
Our production, quality and R&D systems are built in-house with AI. Years of batch records are analysed for patterns. Every finding is reviewed by a chemist before anything changes.
> batch.trace
charge ............ logged
first fraction .... logged
qc gate ........... analyst cleared
collection ........ logged
lot ............... linked to batch
dispatch .......... on time
Reactor to customer, one continuous record
- Reactor charge
- Fraction cuts
- QC gate
- Collection
- Lot release
- Dispatch
In the lab
Years of batch data, working for the next batch.
AI surfaces patterns in yield, purity and performance across our batch history. Chemists review every finding. Any change to a process or formulation goes through formal change control before it reaches production.
98.3%
First-pass grade output
[PERIOD]. Batches meeting target grade specification without reprocessing.
99.1%
On time, in full
FY 2025-26. Orders delivered by the committed date and in the full ordered quantity.
AI builds our systems. Qualified people make every quality decision.
See how we operate
Latest from the laboratory
Free E-Book
The OOS Trap
Why laboratory investigations fail to find a root cause, and the inputs nobody checks.
Purohith Makala, Managing Director
Technical Notes
Why UV cutoff matters in HPLC solvent selection
A solvent that passes a purity assay can still ruin a low-wavelength method. UV cutoff, gradient baseline drift and trace absorbing impurities decide whether a separation is usable.
18 June 2026 · 6 min read
Technical Notes
Reading a certificate of analysis: what actually matters
A COA is a release document, not a marketing sheet. Here is how to read one during vendor qualification, and which fields auditors check first.
27 May 2026 · 5 min read
Industry
Excipient qualification for Indian formulators
Multi-compendial excipients simplify filings only when the supporting documentation is complete. A practical view of what a formulation team should collect before first use.
9 April 2026 · 7 min read
