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SUPELCOSIL™ LC-18-S (5 µm) HPLC Columns

L × I.D. 25 cm × 2.1 mm, HPLC Column

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About This Item

UNSPSC Code:
41115700
eCl@ss:
32110501

product name

Columna para HPLC SUPELCOSIL™ LC-8-S, 5 μm particle size, L × I.D. 25 cm × 2.1 mm

agency

suitable for USP L1

feature

endcapped

manufacturer/tradename

SUPELCOSIL™

extent of labeling

11.0% carbon loading

parameter

≤70 °C temp. range
400 bar pressure (5801 psi)

technique(s)

HPLC: suitable

L × I.D.

25 cm × 2.1 mm

surface area

170 m2/g

surface coverage

surface coverage 3.1 μmol/m2

matrix

silica gel, spherical particle platform

matrix active group

C18 (octadecyl) phase

particle size

5 μm

pore size

120 Å

application(s)

food and beverages

separation technique

reversed phase

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General description

Las columnas SUPELCOSIL LC-18-S están diseñadas para una separación de desoxiribonucleosidos y ribunucleosidos. Cada columna es probada para asegurar su aplicación.

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Legal Information

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC

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Certificados de análisis (COA)

Lot/Batch Number
167159-06
167159-05
167159-04
167159-03
167159-02

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O Cudina et al.
Farmaco (Societa chimica italiana : 1989), 55(2), 125-127 (2000-04-27)
Fluocortolone and its esters are synthetic corticosteroids used topically in the treatment of various skin disorders. A method that can be successfully used for the separation and determination of fluocortolone pivalate and fluocortolone hexanoate in suppositories was developed. This method
G R Granneman et al.
Clinical pharmacokinetics, 29 Suppl 2, 1-8 (1995-01-01)
A rapid and sensitive assay was developed for the measurement of plasma concentrations of zileuton racemate, a potent inhibitor of 5-lipoxygenase. Zileuton and its inactive N-dehydroxylated metabolite were extracted from human, monkey, and rat plasma by use of a solid-phase
V Stocchi et al.
Analytical biochemistry, 167(1), 181-190 (1987-11-15)
A simple and fast ion pair reversed-phase high-performance liquid chromatographic method has been developed for the simultaneous determination of ATP, ADP, AMP, GTP, GDP, IMP, NADP+, NADPH+, NAD+, NADH, ADP-ribose, inosine, adenosine, hypoxanthine, and xanthine. This method allows us to
K M Matar et al.
Therapeutic drug monitoring, 21(5), 559-566 (1999-10-16)
A simple, rapid, sensitive, and reproducible high-performance liquid chromatographic (HPLC) method for simultaneous determination of the antiepileptic drugs (ethosuximide, primidone, lamotrigine, phenobarbital, phenytoin, and carbamazepine) and two metabolites (carbamazepine-diol and carbamazepine-epoxide) in human plasma is described. The procedure involves extraction
V Stocchi et al.
Analytical biochemistry, 146(1), 118-124 (1985-04-01)
A simple and rapid method for the determination of ATP, ADP, AMP, NADP+, NAD+, NADPH, and NADH in human erythrocytes is described. A single-step extraction procedure employing alkaline medium and CF 50A Amicon ultrafiltration membranes allows a simultaneous and total
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