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Merck

PHR1620

Supelco

Fluvastatin sodium

Pharmaceutical Secondary Standard; Certified Reference Material

Sinónimos:

(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
124,00 €

124,00 €


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1 G
124,00 €

About This Item

Fórmula empírica (notación de Hill):
C24H25FNNaO4
Número de CAS:
Peso molecular:
433.45
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

124,00 €


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grado

certified reference material
pharmaceutical secondary standard

Nivel de calidad

Agency

traceable to Ph. Eur. Y0001082
traceable to USP 1285931

familia API

fluvastatin

CofA

current certificate can be downloaded

envase

ampule of 1 × 1 g

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

pharmaceutical (small molecule)

Formato

neat

temp. de almacenamiento

2-30°C

cadena SMILES

[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

Clave InChI

ZGGHKIMDNBDHJB-RPQBTBOMSA-M

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Descripción general

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.

Aplicación

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 al pie de página

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.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Certificados de análisis (COA)

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Fluvastatin Sodium
USP42/NF37: United States Pharmacopeia and National Formulary
United States Pharmacopeia/National Formulary, 43(5), 1972-1972 (2019)
The role of statin drugs in combating cardiovascular diseases-A review
Pichandi S, et al
International journal of current science research, 1(2), 47-56 (2011)
Determination of Fluvastatin Sodium Extended-release Tablets by HPLC
Zhang S, et al.
China Pharmacy, 42(34), 1784-1804 (2007)
Development and validation of stability-indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin, and rosuvastatin in pharmaceuticals
Gomes FP, et al.
Analytical Letters, 42(12), 1784-1804 (2009)
Masao Nishiya et al.
Anti-cancer drugs, 30(5), 451-457 (2019-03-29)
Although vemurafenib has been shown to improve the overall survival of patients with metastatic melanoma harboring the BRAF V600E mutation, its efficacy is often hampered by drug resistance acquired within a relatively short period through several distinct mechanisms. In the

Preguntas

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

    1 respuesta
    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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