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Merck
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1.46679

Millipore

Fluid Thioglycollate Medium + LTH

bottle of, ready-to-use, bottle volume 500 mL , filling volume

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About This Item

Codice UNSPSC:
41106214

agenzia

EP 2.6.1
JP 4.06
USP 71
71

Livello qualitativo

Sterilità

sterile; autoclaved

Forma fisica

liquid

Caratteristiche

closure type screw cap with septum
ready-to-use

Confezionamento

bottle of

Capacità bottiglia

500 mL

Volume del flacone

500 mL , filling volume

pH

7.1±0.2

applicazioni

cosmetics
food and beverages
pharmaceutical
sterility testing

Componenti

(Lecithin, Tween, Histidine)

Temperatura di conservazione

2-25°C

Compatibilità

nonselective for

Descrizione generale

FTM with Neutralizers also known as Fluid Thioglycollate Medium is a nutrient rich complex medium designed to serve as a sterility control for pharmaceutical products.
Thioglycollate and L-Cystine in the medium reduces the redox potential of the medium to create an anaerobic atmosphere. Also, it deactivates the presence of mercury and other heavy metals.
The presence of agar further reduces oxygen diffusion and resazurin indicates the reduced oxygen potential in the medium. An increased oxygen concentration will render a color change from yellow to pink in the medium.
Lecithin and Polysorbate 80, are effective against quaternary ammonium compounds, amphoteric surfactants, benzamidines, chlorhexidines and dequadin. Polysorbate 80 inactivates benzyl alcohol, carbanilides, dichlorbenzyl alcohols, benzoic acid, p-hydroxybenzoic acid and its esters, phenols, phenylethyl alcohols and PHB esters. Histidine is effective against formaldehyde and formaldehyde releasing agents.

Applicazioni

Fluid Thioglycollate Medium is used to isolate and cultivate fastidious anaerobic and aerobic microbes in test samples. FTM is suitable as a sterility control of pharmaceutical products.
Fluid Thioglycollate Medium is recommended for sterility testing of samples according to EU and US pharmacopeia.

Caratteristiche e vantaggi

  • Our ready-to-use media provide the highest level of quality and testing confidence. They are formulated and tested to meet the pharmacopeia requirements.
  • Sterility testing media and rinse solutions are manufactured in an ISO 9001, environmentally controlled production center. Each lot undergoes a stringent quality control (QC) procedure, including pH, sterility, and growth promotion tests.
  • Our manufacturing approach ensures the highest level of clarity for our media and rinsing fluids, thus improving accuracy, and reducing the risk of incorrect interpretation and false results.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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