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Merck
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主要文件

1.46679

Millipore

流体巯基乙酸盐培养基

bottle capacity 500 mL, bottle filling volume 500 mL, closure type, Blue screw cap with septum and protector, pack of 6 bottles

别名:

FTM, FTM with Neutralizers, Fluid Thioglycollate Medium + LTH

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About This Item

分類程式碼代碼:
41106214

agency

EP 2.6.1
JP 4.06
USP 71
71

品質等級

無菌

sterile; autoclaved

形狀

liquid

特點

closure type Blue screw cap with septum and protector
ready-to-use

包裝

pack of 6 bottles

瓶容量

500 mL

bottle filling volume

500 mL

容量

500 mL

pH值

7.1±0.2

應用

cosmetics
food and beverages
pharmaceutical
sterility testing

成分

(with Lecithin, Tween 20, Histidine)

儲存溫度

2-25°C

適合性

nonselective for

一般說明

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.

應用

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.

特點和優勢

  • 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.

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2


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