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58355-U

Supelco

SUPELCOSIL LC-18-DB (5 µm) HPLC Columns

L × I.D. 25 cm × 4.6 mm, HPLC Column

Synonyme(s) :

High Purity C18 HPLC Column

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About This Item

Code UNSPSC :
41115700
eCl@ss :
32110501
Nomenclature NACRES :
SB.52

product name

Colonne HPLC SUPELCOSIL LC-18-DB, 5 μm particle size, L × I.D. 25 cm × 4.6 mm

Matériaux

stainless steel column

Agence

suitable for USP L1

Gamme de produits

SUPELCOSIL

Caractéristiques

endcapped

Fabricant/nom de marque

SUPELCOSIL

Conditionnement

1 ea of

Ampleur du marquage

11.0% Carbon loading

Paramètres

0-70 °C temperature
400 bar pressure (5801 psi)

Technique(s)

HPLC: suitable

L × D.I.

25 cm × 4.6 mm

Superficie

170 m2/g

Couverture de surface

surface coverage 3.1 μmol/m2

Matrice

silica gel, spherical particle platform
fully porous particle

Groupe de la matrice active

C18 (octadecyl) phase

Taille des particules

5 μm

Dimension de pores

120 Å

pH de fonctionnement

2-7.5

Application(s)

food and beverages

Compatibilité

for use with PTC-AA

Technique de séparation

reversed phase

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Catégories apparentées

Description générale

Les phases SUPELCOSIL LC-DB sont spécialement désactivées pour les composés basiques. Ces colonnes se caractérisent par un faible temps de rétention, une meilleure symétrie de pic et une plus grande efficacité pour les bases organiques que toute autre colonne de silice de type A en phase inverse.

Application


  • OPTIMIZATION AND VALIDATION OF HPLC METHOD FOR TETRAMETHRIN DETERMINATION IN HUMAN SHAMPOO FORMULATION.: This study discusses the optimization and validation of a high-performance liquid chromatography (HPLC) method using SUPELCOSIL LC-18-DB HPLC Column for the analysis of tetramethrin in shampoo formulations (Zeric Stosic et al., 2016).

  • Mass spectrometric characterization and HPLC determination of the main urinary metabolites of nimesulide in man.: Details a robust approach for identifying and quantifying nimesulide metabolites via HPLC, underscoring the column′s applicability in complex biological matrices (Carini et al., 1998).


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Informations légales

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

O Majid et al.
Therapeutic drug monitoring, 23(2), 163-168 (2001-04-11)
Recipients of organ transplants remain particularly dependent on prednisolone as part of their maintenance immunosuppression. Despite this, the pharmacokinetics of prednisolone have never been fully characterized in these patients, and consequently dosing remains empirical. Accurate monitoring of prednisolone, its primary
S L Bramer et al.
Journal of pharmaceutical and biomedical analysis, 26(4), 637-650 (2001-08-23)
An LC/MS/MS method for the simultaneous determination of cilostazol, a quinolinone derivative, and three active metabolites, OPC-13015, OPC-13213, and OPC-13217, in human plasma was developed and validated. Cilostazol, its metabolites, and the internal standard, OPC-3930 were extracted from human plasma
Xinghua Sun et al.
Anticancer research, 25(1A), 59-62 (2005-04-09)
A rapid, sensitive and specific high-performance liquid chromatographic (HPLC) method for the separation and quantification of L-methionine in plasma has been developed. After derivatization of plasma amino acids with o-phthalaldehyde (OPA), a 50 microl sample was loaded on a reversed-phase
E Terjéki et al.
Journal of pharmaceutical and biomedical analysis, 24(5-6), 913-920 (2001-03-15)
RGH-1756 (1-(2-methoxy-phenyl)-4-(4-[4-(6-imidazo[2,1-b]-thiazolyl)-phenoxy]-butyl)-piperazine dimethansulphonate) is a novel atypical antipsychotic candidate of Gedeon Richter Ltd. A new HPLC method has been developed and validated for the quantitative determination of RGH-1756 in dog and rat plasma. The compound and the internal standard are
P K Kunicki
Journal of chromatography. B, Biomedical sciences and applications, 755(1-2), 331-335 (2001-06-08)
A HPLC-UV determination of loratadine in human plasma is presented. After simple liquid-liquid extraction with 2-methylbutane-hexane (2:1) and evaporation of organic phase the compounds were re-dissolved in 0.01 M HCl, evaporated again and finally separated on a Supelcosil LC-18-DB column.

Protocoles

Amino Acid Analysis is the suitable tool for precise determination of protein quantities but also provides detailed information regarding the relative amino.

Chromatograms

application for SPE, application for HPLC

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