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59560

Supelco

SUPELCOSIL LC-Si Supelguard Cartridge

5 μm particle size, L × I.D. 2 cm × 4 mm

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eCl@ss:
32110501

agency

suitable for USP L3

Quality Level

packaging

pkg of 2 ea

technique(s)

HPLC: suitable

L × I.D.

2 cm × 4 mm

matrix active group

silica phase

particle size

5 μm

pore size

120 Å

application(s)

food and beverages

compatibility

use to protect LC-Si, LC-3Si

separation technique

hydrophilic interaction (HILIC)
normal phase

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This Item
595505956759558
particle size

5 μm

particle size

5 μm

particle size

5 μm

particle size

5 μm

matrix active group

silica phase

matrix active group

silica phase

matrix active group

cyano phase

matrix active group

amino phase

agency

suitable for USP L3

agency

suitable for USP L3

agency

suitable for USP L10

agency

suitable for USP L8

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

technique(s)

HPLC: suitable

pore size

120 Å

pore size

120 Å

pore size

120 Å

pore size

120 Å

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Legal Information

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC
Supelguard is a trademark of Sigma-Aldrich Co. LLC

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R Lovlin et al.
Journal of chromatography. B, Biomedical applications, 679(1-2), 196-198 (1996-04-26)
The stereospecific HPLC assays reported for ketoprofen (KT) mainly utilize indirect approaches. These assays involve the formation of amide diastereomeric derivatives, which are then separated by chromatography. The advantages of indirect methods include versatility, good sensitivity and cost effectiveness; however
Mohammed Shahid Ali et al.
Journal of pharmaceutical and biomedical analysis, 43(1), 158-167 (2006-08-05)
A new HILIC method has been developed for the simultaneous determination of pseudoephedrine hydrochloride (PSH), diphenhydramine hydrochloride (DPH) and dextromethorphan hydrobromide (DXH) in cough-cold syrup. Mobile phase consists of methanol:water (containing 6.0 g of ammonium acetate and 10 mL of
J J Agren et al.
Lipids, 37(6), 613-619 (2002-07-18)
Normal-phase HPLC resolution of sn-1,2(2,3)- and x-1,3-DAG generated by partial Grignard degradation from natural TAG was carried out with both (R)-(-) and (S)-(+)-1-(1-naphthyl)ethylurethane derivatives. The diastereomeric sn-1,2- and sn-2,3-DAG derivatives were resolved using two Supelcosil LC-Si (5 microm, 25 cm

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