Analysis · Purification · Consumables

From complex sample to pure answer.

HIPSOUL is an integrated analytical & purification solutions provider. One laboratory partner for HPLC/UHPLC analysis, method development, impurity identification, preparative purification, reference standards — and the columns and consumables to run them.

2000+Projects delivered
99.5%Max purity achieved (HPLC)
48hTypical first response
HIPSOUL · LC RUN #A-2261
mAU t (min) 2.0 4.0 6.0 8.0 1 · 1.82 2 · 4.07 ★ 3 · 5.93 4 · 7.66
C18 · 4.6 × 250 mm · 5 µm UV 254 nm 1.0 mL/min
GMP-aligned workflows
ICH-guided impurity studies
Analytical-grade laboratory
Method validation support
Full data & report package
mg → multi-gram scale-up
NDA-protected projects
What problem are you solving?

Every difficult sample has a bottleneck. Pick yours.

Select the challenge closest to your project — we’ll point you to the HIPSOUL capability that removes it.

HIPSOUL
ONE PARTNER
01Analysis 02Method Dev 03Purification 04Preparation 05Standards 06Consumables
One partner solution

Stop coordinating four vendors. Brief one team.

Analysis, method development, purification, standard preparation and consumables usually live with different suppliers — each hand-off costing time, context and sample. At HIPSOUL they share one lab, one project owner and one report chain.

  • Continuity of sample knowledge. The chemist who analyzed your sample plans its purification.
  • Methods that transfer. Analytical methods are developed on the same phases we supply as columns.
  • One commercial relationship. Single quote, single NDA, single point of accountability.
Analytical services

Answers you can put in a report — or a filing.

HPLC/UHPLC and LC-MS based analytical work, delivered with full chromatograms, raw data and documented conditions. Hover any card for scope.

AS-01

Method Development

Robust, transferable HPLC/UHPLC methods built for your matrix and your instruments.

  • Phase & gradient screening
  • Forced degradation fit
  • Validation-ready SOP
AS-02

Impurity Identification

Isolation and structural characterization of unknown and related substances.

  • LC-MS profiling
  • Impurity enrichment
  • ICH Q3A/Q3B context
AS-03

Sample Testing

Assay, purity, content uniformity and related-substance testing for routine and project work.

  • Per-batch or campaign
  • Client or pharmacopoeial methods
  • Fast COA-style reporting
AS-04

HPLC / UHPLC Analysis

High-resolution separations on modern instruments with a deep column library.

  • RP, NP, HILIC, chiral
  • Sub-2 µm UHPLC
  • Full audit-trail data
Purification services

From crude mixture to single peak.

Preparative chromatography from milligram screening to multi-gram delivery — for natural products, drug impurities and difficult synthetic mixtures.

PS-01

Natural Product Purification

Target isolation from plant extracts, fermentation broths and complex biological matrices.

  • Extract pre-fractionation
  • Orthogonal polishing
  • Structure confirmation
PS-02

Drug Impurity Purification

Enrichment and isolation of trace impurities at the quantities your tox and ID work needs.

  • From <0.1% area peaks
  • mg-level recovery
  • Purity COA included
PS-03

Preparative Chromatography

Analytical-to-prep scale-up with documented loading studies and recovery data.

  • Up to multi-gram scale
  • Focused fraction collection
  • Solvent-exchange & drying
PS-04

Compound Isolation

Recovery of single components from reaction mixtures, degradation studies and process streams.

  • Unknowns welcome
  • Stability-aware handling
  • Identity package on request

Drag to purify

CRUDE EXTRACT → ISOLATED TARGET  |  Purity: 41.2%
TARGET · 99.5%
Crude samplePurified compound
Preparation services

Reference materials, prepared to order.

When the standard you need doesn’t exist in a catalog, we isolate, purify and characterize it for you.

RP-01

Reference Standard Preparation

Working and secondary reference standards with assigned purity and full characterization data.

  • HPLC purity assignment
  • MS / NMR identity data
  • Stability guidance
RP-02

Control Sample Preparation

QC control and system-suitability samples matched to your method and matrix.

  • Batch-to-batch consistency
  • Custom concentrations
  • Documented preparation
RP-03

Custom Compound Preparation

Milligram-to-gram quantities of impurities, metabolite analogs and rare natural products.

  • Isolation or semi-synthesis route
  • Purity to specification
  • COA with every shipment
HPLC / UHPLC consumables

The hardware behind every clean baseline.

Columns and flow-path consumables manufactured to tight QC — the same parts our own laboratory runs every day.

HPLC & UHPLC Columns

C18/C8, HILIC, phenyl and specialty phases; 1.8–10 µm; analytical to prep dimensions.

Request column list →

Guard Columns

Analytical and preparative guard cartridges and holders that extend main-column lifetime.

Analytical & prep →

Inline Filters

Pre-column inline filters, 0.5–2 µm frits, protecting UHPLC systems from particulates.

0.5 / 1 / 2 µm →

Stainless Steel Tubing

Pre-cut and coiled 316 SS HPLC tubing in standard IDs, deburred and passivated.

Custom lengths →

Solvent Inlet Filters

Mobile-phase inlet filters in SS and PEEK, 2–20 µm, for clean solvent delivery.

SS & PEEK →

Empty Columns

Empty column hardware for self-packing — tubes, frits and end fittings, analytical to prep.

Self-pack hardware →

Fittings & Connectors

Ferrules, unions, nuts and adapters in SS and PEEK for leak-free flow paths.

Full catalog →

OEM & Custom Programs

Private-label packing, custom dimensions and recurring-supply agreements for labs and distributors.

Talk to sales →
Laboratory capability

Real instruments. Real throughput. Real data.

Your project runs on a working analytical and preparative laboratory — not a brokered network.

12+LC systems online
300+Column phases in library
99.5%Max delivered purity
5 g+Single-run prep capacity

HPLC

Quaternary and binary systems with UV/DAD detection for routine and project analysis.

UHPLC

Sub-2 µm separations at high pressure for speed, resolution and low solvent burn.

Preparative HPLC

Semi-prep to prep-scale systems with high-flow pumps and large-ID column hardware.

LC-MS

Mass-directed identification of unknowns, impurities and co-eluting components.

Fraction Collection

Time-, threshold- and mass-triggered collection for clean cuts on every prep run.

Sample Preparation

Extraction, filtration, SPE and dilution workflows matched to your matrix.

Method Validation

Specificity, linearity, accuracy, precision and robustness studies to ICH Q2.

Solvent Recovery & Drying

Rotary evaporation and lyophilization to deliver purified compounds shipment-ready.

Data & Reporting

Audit-trailed CDS data, full chromatograms and bilingual (EN/中文) project reports.

Industries served

Built for laboratories that answer to auditors.

Pharmaceutical R&D
CRO / CDMO
Universities & Institutes
Natural Products
Food Testing Labs
Chemical & Biotech
How a project runs

Five steps from sample to deliverable.

STEP 1 · DAY 0

Sample Submission

Ship under NDA with our simple submission form; we confirm receipt and condition same day.

STEP 2 · DAY 1–2

Technical Evaluation

A chemist screens your sample and returns a written approach, timeline and fixed quote.

STEP 3

Method Development

Phase and condition screening until separation, recovery and robustness meet target.

STEP 4

Analysis / Purification

Production runs with in-process checks; you receive progress updates, not silence.

STEP 5

Report & Delivery

Full report, raw data and — for purification — your compound with purity COA.

Application scenarios

What this looks like in practice.

Representative projects — details anonymized under NDA. Ask for the application note closest to your problem.

Impurity separation · Pharma QC

Co-eluting impurity resolved and identified before a regulatory deadline

A 0.18% shoulder peak in an API related-substances method was baseline-resolved on an alternative phase, enriched by prep-HPLC and identified by LC-MS — with enough material recovered for the client’s reference file.

0.18%Starting peak area
12 mgImpurity isolated
3 wksSample to report
Natural product purification

Multi-gram isolation of a bioactive compound from plant extract

A two-stage preparative strategy — reversed-phase capture followed by orthogonal polishing — took a 23%-pure enriched extract to a single-peak product, delivered dried with full chromatographic data.

99.2%Final purity
4.6 gDelivered
87%Step recovery
Method optimization · CRO transfer

A 38-minute legacy method rebuilt as a 9-minute UHPLC method

Phase re-screening and gradient redesign cut run time by 76% while improving resolution of the critical pair — validated for specificity and precision, then transferred with a written protocol.

−76%Run time
R>2.0Critical pair
2 sitesTransferred
Preparative scale-up

Milligram screen to multi-gram campaign without changing selectivity

Loading studies on analytical hardware predicted prep behavior on the same phase chemistry; the campaign scaled 400× with no re-development and consistent fraction purity across batches.

400×Scale factor
0Methods re-developed
6Batches delivered
Why HIPSOUL

Six reasons technical buyers choose us.

W-01

Analysis + purification, integrated

The team that characterizes your sample designs and runs its purification — no translation loss between vendors.

W-02

Real laboratory capability

Work happens on our own HPLC, UHPLC, prep-LC and LC-MS instruments, with capacity we control.

W-03

Custom by default

Every project gets its own approach document. We don’t force your sample into a standard package.

W-04

Fast, committed response

Technical reply within 48 hours, written timelines, and proactive updates while your project runs.

W-05

Engineer-level support

Your contact is a chromatographer, not a ticket queue — in English or Chinese, your choice.

W-06

Consumables + services together

Methods we develop run on columns we supply, so what works in our lab keeps working in yours.

Frequently asked

Before you submit a sample

What sample types can you handle?

Small-molecule APIs and intermediates, plant and natural-product extracts, fermentation products, food and chemical matrices, and synthetic reaction mixtures. If you’re unsure, describe the sample in your inquiry — evaluation is free and confidential.

Can you develop custom HPLC methods?

Yes — method development is a core service. We screen phases and conditions against your acceptance criteria, document the final method as a transferable SOP, and can support validation to ICH Q2 if required.

Can you purify unknown compounds?

Yes. We routinely isolate unidentified peaks and unknown components, using LC-MS to track the target through purification. Structural characterization data can be included in the deliverable.

Can you provide preparative chromatography?

Yes — from semi-prep isolation of milligram quantities to multi-gram campaigns, with loading studies, fraction analysis, solvent exchange and drying handled in-house.

Do you supply columns and consumables?

Yes. HIPSOUL manufactures and supplies HPLC/UHPLC columns, guard columns, inline filters, tubing, solvent inlet filters, empty column hardware and fittings — including OEM and custom-dimension programs.

How do I submit samples?

Start with the inquiry form below or email our technical team. We’ll sign an NDA if needed, send a submission form and shipping instructions, and confirm receipt and sample condition the day your package arrives.

Start a project

Have a complex sample, a difficult impurity, or a purification challenge?

Send a short description. A HIPSOUL chromatographer — not a sales bot — replies with a technical approach within 48 hours.

NDA available · EN / 中文 · Free technical evaluation

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