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PHR1620

Supelco

Fluvastatin sodium

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

(3R,5S,6E)-rel-7-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid monosodium salt

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1 G
125,00 €

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Cambia visualizzazione
1 G
125,00 €

About This Item

Formula empirica (notazione di Hill):
C24H25FNNaO4
Numero CAS:
Peso molecolare:
433.45
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

125,00 €


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Grado

certified reference material
pharmaceutical secondary standard

Livello qualitativo

agenzia

traceable to Ph. Eur. Y0001082
traceable to USP 1285931

Famiglia di API

fluvastatin

CdA

current certificate can be downloaded

Confezionamento

ampule of 1 × 1 g

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

[Na+].CC(C)n1c(\C=C\[C@H](O)C[C@H](O)CC([O-])=O)c(-c2ccc(F)cc2)c3ccccc13

InChI

1S/C24H26FNO4.Na/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30;/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30);/q;+1/p-1/b12-11+;/t18-,19-;/m0./s1
ZGGHKIMDNBDHJB-RPQBTBOMSA-M

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Descrizione generale

Fluvastatin sodium is a lipid-lowering drug that belongs to the group of compounds known as statins. It acts by inhibiting the enzyme HMG-CoA reductase that plays a key role in the cholesterol production. It is generally used to reduce plasma cholesterol levels and prevent cardiovascular disease.[1]
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Applicazioni

Fluvastatin sodium may be used as a reference standard for the determination of the analyte in bulk drug and pharmaceutical formulations by high performance liquid chromatography.[2][3][4]
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Nota a piè di pagina

To see an example of a Certificate of Analysis for this material enter LRAA5290 in the slot below. This is an example certificate only and may not be the lot that you receive.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Domande

  1. What is the best method for reconstituting PHR1620-1G Fluvastatin sodium, which arrived in powder form?

    1 risposta
    1. Fluvastatin Sodium is a hygroscopic powder that is soluble in alcohol, methanol, and water. For testing purposes, it recommends preparing a sample solution of 0.5 mg/mL of Fluvastatin Sodium. This involves dissolving the powder first in Solution B, using 40% of the final volume, and then diluting it with Solution A to reach the final volume. Solution A is prepared by adding 20 mL of 25% aqueous tetramethylammonium hydroxide solution to 880 mL of water, adjusting the pH to 7.2 + 0.2 with phosphoric acid, and adding 100 mL of a mixture of methanol and acetonitrile (60:40). Solution B is prepared by adding 20 mL of 25% aqueous tetramethylammonium hydroxide solution and 80 mL of water to 900 mL of a mixture of methanol and acetonitrile (60:40), also adjusting the pH to 7.2 + 0.2 with phosphoric acid.

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