

UV-Vis Spectrophotometer
紫外可见分光光度计
- SKU SPC-0001
- Spectrometers
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Spectral bandwidth | 2 nm |
| Wavelength accuracy | ±0.3 nm |
| Photometric range | −3 to 3 A |
| Photometric accuracy | ±0.003 A at 1 A |
| Stray light | ≤0.05% T at 220 nm |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <857>, Ph. Eur. 2.2.25, ASTM E275
What is the UV-Vis Spectrophotometer?
A UV-Vis spectrophotometer measures light absorbed by a sample across the ultraviolet and visible range. It is the standard optical instrument for concentration measurement, colorimetric assays and identity testing in analytical, pharmaceutical and environmental laboratories.
What is the UV-Vis Spectrophotometer?
A UV-Vis spectrophotometer measures light absorbed by a sample across the ultraviolet and visible range. It is the standard optical instrument for concentration measurement, colorimetric assays and identity testing in analytical, pharmaceutical and environmental laboratories.
Overview
A UV-Vis spectrophotometer uses a deuterium lamp for the ultraviolet and a tungsten-halogen lamp for the visible range, combined through a monochromator or grating to select a narrow wavelength band. A single-beam design references the blank manually, while a double-beam design splits light between sample and reference for better baseline stability over long runs. Detectors are typically silicon photodiodes or photodiode arrays. Performance is described by wavelength range, spectral bandwidth, photometric accuracy and stray-light level. The instrument reports absorbance, transmittance or concentration after a calibration curve is applied. Stray light and baseline stability limit accuracy at high absorbance.
How does it work?
A spectrometer collects light from a source or sample and disperses it with a prism, diffraction grating or interferometer. The separated wavelengths fall on a detector, usually a photodiode, charge-coupled device or photomultiplier, which converts intensity into an electrical signal. The signal is digitized and plotted as intensity versus wavelength or wavenumber. Transmission, absorbance or emission bands reveal molecular or atomic structure, because specific groups absorb or emit at characteristic wavelengths. Optical resolution depends on slit width, grating groove density and detector pixel size, while sensitivity depends on source brightness, optical throughput and detector quantum efficiency. Wavelength calibration against emission lamps or reference standards keeps readings accurate and comparable between instruments.
What are the key features?
- Deuterium and tungsten-halogen lamps with automatic wavelength switching
- Czerny-Turner monochromator for stable spectral bandwidth
- Photometric range covering about negative 3 to 3 absorbance
- Graphical software for calibration curves and multi-wavelength measurement
- USB and LAN interfaces for data export and compliance records
What are the technical specifications?
A typical uv-vis spectrophotometer configuration offers wavelength range of 190–1100 nm, spectral bandwidth of 2 nm, wavelength accuracy of ±0.3 nm, photometric range of −3 to 3 A, photometric accuracy of ±0.003 A at 1 A and stray light of ≤0.05% T at 220 nm. 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 UV-Vis Spectrophotometer is used in pharmaceutical assay and identity testing, water and wastewater analysis, food additive and colour measurement and biochemical protein and nucleic acid assays. Across the wider Spectrometers class, laboratories also deploy it for pharmaceutical identity and content testing, chemical reaction monitoring and optical coating and filter characterization.
Which standards and certifications apply?
Relevant standards and methods include USP <857>, Ph. Eur. 2.2.25, ASTM E275, ASTM E958 and JP 2.24. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install spectrometers on a stable bench away from vibration and large temperature swings, and allow warm-up for source and detector stability. Protect optics from dust and humidity; hygroscopic components such as KBr windows need desiccation or purging. Establish a calibration schedule covering wavelength accuracy, photometric accuracy and stray light, using traceable filters or lamps. Keep reference spectra and performance records for trend analysis. For regulated work, define user access, audit trails and electronic records, and document installation, operational and performance qualification. Regular lamp replacement and cleaning of sample compartments reduce drift.
How do I select the right UV-Vis Spectrophotometer?
Select a UV-Vis instrument when the method requires absorbance or transmittance in the ultraviolet or visible region. Choose a double-beam model for long unattended runs or unstable sources, and a fixed-bandwidth instrument when the pharmacopoeial method specifies a set bandwidth. In an RFQ state the wavelength range, bandwidth, photometric accuracy, cell type and required software compliance features.
How does it compare with other Spectrometers variants?
Choose by measurand first: absorption in the ultraviolet and visible suits a UV-Vis spectrophotometer, trace fluorescence suits a fluorescence spectrometer, non-contact identification of solids and liquids suits a Raman spectrometer, functional-group analysis of solids and liquids suits an FTIR spectrometer, and rapid reflectance or transmission measurements suit a CCD array spectrometer. Then match spectral range, resolution and stray-light performance to the method. Consider whether a double-beam or array design is needed, the required detector sensitivity, and whether a flow cell, fibre probe or integrating sphere is required. Check wavelength accuracy, baseline stability, software for spectral libraries and data integrity, and available calibration standards before specifying.
Full specifications
| Wavelength range | 190–1100 nm |
|---|---|
| Spectral bandwidth | 2 nm |
| Wavelength accuracy | ±0.3 nm |
| Photometric range | −3 to 3 A |
| Photometric accuracy | ±0.003 A at 1 A |
| Stray light | ≤0.05% T at 220 nm |
| Detector | Silicon photodiode |
| Light source | Deuterium and tungsten-halogen |
| Baseline flatness | ±0.001 A |
| Data interface | USB, LAN |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Pharmaceutical assay and identity testing
- Water and wastewater analysis
- Food additive and colour measurement
- Biochemical protein and nucleic acid assays
Key features
- Deuterium and tungsten-halogen lamps with automatic wavelength switching
- Czerny-Turner monochromator for stable spectral bandwidth
- Photometric range covering about negative 3 to 3 absorbance
- Graphical software for calibration curves and multi-wavelength measurement
- USB and LAN interfaces for data export and compliance records
Frequently asked questions about UV-Vis Spectrophotometer
A single-beam instrument measures the blank and sample sequentially, which is simple and economical but drifts with source ageing. A double-beam instrument splits light between sample and reference continuously, giving a more stable baseline and better performance for kinetic or long measurements.
Quartz cuvettes are required below about 340 nm because glass absorbs ultraviolet light. Glass or polystyrene cuvettes are adequate for the visible range. For quantitative work, match cuvettes for path length and optical quality and use the same type for blank and sample.
Stray light is unwanted radiation reaching the detector at wavelengths outside the selected band. It is reduced by good monochromator design, an order-sorting filter and a clean optical path, and is verified with cutoff filters or reference solutions. Low stray light is important for accurate measurement at high absorbance.
Concentration is usually measured with a UV-Vis spectrophotometer, because absorbance follows the Beer–Lambert law and many compounds absorb strongly in the ultraviolet. Fluorescence spectrometers offer lower detection limits for fluorescent analytes. The correct choice depends on the analyte, matrix and required limit of detection.
Spectral resolution is the smallest wavelength difference the instrument can separate, set by slit width, grating and detector. Higher resolution distinguishes closely spaced bands and sharp peaks but reduces light throughput. Choose resolution that matches the narrowest feature the method must resolve.
Yes. Wavelength accuracy drifts with lamp ageing, mechanical change and temperature. Calibration uses emission lines from deuterium or mercury lamps, or certified reference filters, and is verified against defined tolerances. Records of wavelength, photometric and stray-light checks support traceability.
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