1.05914
HPTLC plates, Silica gel 60 RP-18
pkg of 25 plates, plate L × W 20 cm × 10 cm, glass support
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About This Item
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material
glass support
silica gel 60 matrix
Quality Level
feature
binder Organic Polymer
fluorescent indicator: no
packaging
pkg of 25 plates
technique(s)
thin layer chromatography (TLC): suitable
layer thickness
200 μm
plate L × W
20 cm × 10 cm
particle size
5-6 μm
pore size
60 Å medium pore diameter
storage temp.
2-30°C
Related Categories
General description
25 Glass plates 20 x 10 cm
RP modified plates serve two purposes: act as a pilot method for HPLC and allow to choose various solvent system for special separations. Our RP-modified silica layers are well suited for many separation challenges that unmodified silica cannot overcome. These layers use aqueous solvent systems to separate extremely non-polar substances and analyze particular polar substances that can adapt to ion-pair chromatography. What’s more, RP-modified silica layers are less dependent on atmospheric humidity. Unlike unmodified silica, RP-phases do not exhibit catalytic activity. This makes them the plates of choice for unstable substance that tend to experience oxidative degradation.
Application
- Densitometric HPTLC method for qualitative, quantitative analysis and stability study of Coenzyme Q10 in pharmaceutical formulations utilizing normal and reversed-phase silica gel plates.: This study presents a high-performance thin-layer chromatography (HPTLC) method for analyzing Coenzyme Q10 in pharmaceutical formulations. The method employs both normal and reversed-phase silica gel plates to achieve qualitative and quantitative analysis, as well as stability testing of Coenzyme Q10 (Abdel-Kader et al., 2016).
- Simultaneous Quantification of Gymnemic Acid as Gymnemagenin and Charantin as β-Sitosterol Using Validated HPTLC Densitometric Method.: This research develops a validated HPTLC densitometric method for the simultaneous quantification of gymnemic acid and charantin in herbal formulations. The method utilizes silica gel 60 F₂₅₄ plates for effective separation and quantification (Ahamad et al., 2015).
- Estimation of catechin in Ayurvedic oil formulations containing Acacia catechu.: The study estimates the content of catechin in Ayurvedic oil formulations using HPTLC. Silica gel 60 F₂₅₄ plates are employed to ensure accurate quantification of catechin in these formulations (Dubey et al., 2009).
- Development and validation of HPTLC method for estimation of tacrolimus in formulations.: This paper details the development and validation of an HPTLC method for estimating tacrolimus in pharmaceutical formulations. The method uses silica gel 60 F₂₅₄ plates for efficient separation and quantification of tacrolimus (Borhade et al., 2009).
- Estimation of berberine in ayurvedic formulations containing Berberis aristata.: The research focuses on the estimation of berberine in Ayurvedic formulations. Using HPTLC with silica gel 60 F₂₅₄ plates, the study provides a reliable method for berberine quantification (Rout et al., 2008).
Linkage
Replaces: 5914-6; 5914
Analysis Note
Specific surface area (according to BET; 5-Pt. measurement): 480 - 540 m²/g
Pore volume (N₂-isotherm): 0.74 - 0.84 ml/g
d 50 (laser diffraction, size distribution): 5 - 7 µm
Layer thickness: 150 - 200 µm
Deviation of layer thickness per plate: ≤ 35 µm
Chromatographic testings:
A) Cholesterin test
hRf-values
- cholesterin, cholesterin test:
13 - 23
B) Steroid test
- methyltestosterone, steroid test: 20 - 35
- Reichstein S, steroid test: 50 - 65
- hydrocortisone, steroid test: 65 - 80
Typical value determined on an activated plate (120°C, 15 min)
Eluent a) aceton/ water (95/5 v/v)
Eluent b) acetonitrile/ water (70/30 v/v)
Pore volume (N₂-isotherm): 0.74 - 0.84 ml/g
d 50 (laser diffraction, size distribution): 5 - 7 µm
Layer thickness: 150 - 200 µm
Deviation of layer thickness per plate: ≤ 35 µm
Chromatographic testings:
A) Cholesterin test
hRf-values
- cholesterin, cholesterin test:
13 - 23
B) Steroid test
- methyltestosterone, steroid test: 20 - 35
- Reichstein S, steroid test: 50 - 65
- hydrocortisone, steroid test: 65 - 80
Typical value determined on an activated plate (120°C, 15 min)
Eluent a) aceton/ water (95/5 v/v)
Eluent b) acetonitrile/ water (70/30 v/v)
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