

Binary UHPLC System
二元超高效液相色谱系统
- SKU UHP-0001
- UHPLC
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- RoHS (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Maximum operating pressure | 100 MPa (1000 bar) |
|---|---|
| Flow rate range | 0.01–2 mL/min |
| Dwell volume | 35–100 µL |
| Gradient composition precision (RSD) | ≤0.1% |
| Flow precision (RSD) | ≤0.05% |
| Injection cycle time | ≤20 s |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <621>, Ph. Eur. 2.2.46, USP <1058>
What is the Binary UHPLC System?
A binary UHPLC system combines two high-pressure pumps rated to about 1000 bar with low dwell volume and low-dispersion plumbing. It is the standard choice for fast reversed-phase gradients on sub-2 µm columns, suited to pharmaceutical impurity profiling and high-throughput quality control where run time matters.
What is the Binary UHPLC System?
A binary UHPLC system combines two high-pressure pumps rated to about 1000 bar with low dwell volume and low-dispersion plumbing. It is the standard choice for fast reversed-phase gradients on sub-2 µm columns, suited to pharmaceutical impurity profiling and high-throughput quality control where run time matters.
Overview
The binary UHPLC configuration mixes two solvents after pressurization, giving dwell volumes of roughly 35–100 µL and gradient delay of well under a minute. Pumps deliver 0.01–2 mL/min up to 1000 bar, and a 1–2 µL flow cell diode-array detector samples at up to 100 Hz. An autosampler with fast needle wash and cycle times under 20 seconds keeps injection overhead low, and a column oven with active solvent pre-heating minimizes thermal mismatch that widens peaks. Typical columns are 2.1 × 50–100 mm packed with 1.7–1.9 µm particles, although 2.7 µm core-shell columns are also used. The system is well suited to impurity methods with gradient times of 3–10 minutes, stability-indicating assays and method transfer from conventional HPLC. Because only two solvents are available, pH and modifier scouting requires manual reservoir changes.
How does it work?
UHPLC follows the same partition principle as HPLC but exploits the van Deemter relationship: smaller particles reduce eddy diffusion and mass-transfer resistance, so efficiency stays high at higher linear velocities. Columns of 1.7–1.9 µm particles, commonly 2.1 mm internal diameter and 50–150 mm long, generate backpressures of several hundred bar, which requires pumps, valves and injectors rated to 1000 bar or more. Extra-column dispersion must be minimized with narrow-bore tubing, low-volume mixers and flow cells of 1–2 µL, otherwise the narrow peaks, often 1–3 seconds wide, are broadened. Fast detector sampling rates of 40–200 Hz are needed to define peaks, and column ovens with active pre-heating control frictional heating. Mobile phases are filtered to 0.2 µm to protect frits. Runs that took 30 minutes on HPLC can often finish in 3–10 minutes.
What are the key features?
- High-pressure binary mixing with dwell volume of roughly 35–100 µL for rapid gradient response
- Pressure rating of 1000 bar enabling 1.7 µm particles on 100–150 mm columns
- Diode-array detector with 1–2 µL flow cell and acquisition rate up to 100 Hz
- Autosampler cycle time under 20 seconds with programmable needle wash to limit carryover
- Active solvent pre-heating in column compartment minimizing frictional heating effects on efficiency
What are the technical specifications?
A typical binary uhplc system configuration offers maximum operating pressure of 100 MPa (1000 bar), flow rate range of 0.01–2 mL/min, dwell volume of 35–100 µL, gradient composition precision (RSD) of ≤0.1%, flow precision (RSD) of ≤0.05% and injection cycle time of ≤20 s. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Binary UHPLC System is used in pharmaceutical impurity profiling, high-throughput QC release testing, stability-indicating assays and method transfer from HPLC. Across the wider UHPLC class, laboratories also deploy it for high-throughput pharmaceutical impurity profiling, multi-residue pesticide and veterinary drug screening and bioanalytical PK sample analysis.
Which standards and certifications apply?
Relevant standards and methods include USP <621>, Ph. Eur. 2.2.46, USP <1058>, ICH Q2(R2), ChP 0512, IEC 61010-1, ISO/IEC 17025 and 21 CFR Part 11. Certification candidates for this model are CE, ISO 9001 manufacturing and RoHS; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Use LC-MS grade solvents and filter samples to 0.2 µm, since particulates quickly block sub-2 µm frits. Replace inlet filters, seals and rotor seals on the manufacturer schedule because pressure cycling wears them faster than in HPLC. Keep tubing from injector to detector short and narrow, and use zero-dead-volume fittings rated for the operating pressure. Qualify the system following USP <1058> and verify detector sampling rate and gradient accuracy. When transferring HPLC methods, follow the allowable adjustments in USP <621>. Observe safety precautions for high-pressure components and never exceed column pressure limits, which are often 1000 bar for UHPLC columns.
How do I select the right Binary UHPLC System?
Select a binary UHPLC when your priority is speed and sharp gradients on 2.1 mm columns. If you screen many buffers and modifiers, consider the quaternary variant. If you need pressures beyond 1000 bar, choose the 1300-bar model. In an RFQ state pressure rating, dwell volume, detector data rate, autosampler cycle time and software compliance features.
How does it compare with other UHPLC variants?
The decisive parameters are pressure rating, dwell and extra-column volume, detector speed and whether methods will be transferred from legacy HPLC. A 600-bar system suffices for 2.7 µm solid-core columns; true sub-2 µm work on 100–150 mm columns calls for 1000–1300 bar. Binary pumps give low dwell volume for fast gradients, while quaternary designs suit screening and pH scouting at modest throughput cost. Micro-flow systems increase mass sensitivity for limited samples and mass spectrometer coupling. Two-dimensional configurations address complex matrices. Also evaluate autosampler cycle time and carryover, because fast runs make injection overhead a large share of total time. Confirm that the software supports method translation with dwell-volume compensation and that data integrity features meet your regulatory requirements.
Full specifications
| Maximum operating pressure | 100 MPa (1000 bar) |
|---|---|
| Flow rate range | 0.01–2 mL/min |
| Dwell volume | 35–100 µL |
| Gradient composition precision (RSD) | ≤0.1% |
| Flow precision (RSD) | ≤0.05% |
| Injection cycle time | ≤20 s |
| Injection carryover | ≤0.005% |
| Detector flow cell volume | 1–2 µL |
| Detector data rate | up to 100 Hz |
| Column oven range | 5–90 °C |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Pharmaceutical impurity profiling
- High-throughput QC release testing
- Stability-indicating assays
- Method transfer from HPLC
Key features
- High-pressure binary mixing with dwell volume of roughly 35–100 µL for rapid gradient response
- Pressure rating of 1000 bar enabling 1.7 µm particles on 100–150 mm columns
- Diode-array detector with 1–2 µL flow cell and acquisition rate up to 100 Hz
- Autosampler cycle time under 20 seconds with programmable needle wash to limit carryover
- Active solvent pre-heating in column compartment minimizing frictional heating effects on efficiency
Frequently asked questions about Binary UHPLC System
Not always. Columns with 2.7 µm core-shell particles reach high efficiency below 600 bar. A 1000-bar rating is needed for 1.7 µm fully porous particles on 100–150 mm columns at optimal flow, and it leaves pressure headroom when using viscous mobile phases such as methanol and water.
Extra-column volume from tubing, fittings, injector loops and detector cells is the main cause. Large-bore tubing, poorly seated fittings and standard 10 µL flow cells can widen peaks enough to lose the resolution gained from small particles. Use low-dispersion kits and verify with a plate count test.
A typical impurity gradient on a 2.1 × 100 mm, 1.7 µm column completes in 5–10 minutes including re-equilibration, compared with 30–60 minutes on a conventional 4.6 × 250 mm HPLC column. Very fast screening methods run in under 2 minutes.
UHPLC uses sub-2 µm particles and hardware rated above 600 bar, typically 1000–1300 bar, which gives narrower peaks, higher resolution and runs three to ten times faster than conventional HPLC. It also requires lower system dispersion and faster detector sampling.
Usually yes. Keep the stationary phase chemistry, scale column length to particle size ratio, adjust flow rate and gradient time proportionally, and compensate for dwell volume differences. USP <621> defines permitted adjustments, but changes beyond those limits require revalidation.
Generally yes. Shorter columns of narrower internal diameter and faster runs typically reduce solvent use per sample by 60–90% compared with a 4.6 × 250 mm HPLC method. The saving depends on whether the method is fully redeveloped on a 2.1 mm column.
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