1.46631
Fluid Thioglycollate Medium
bottle of, ready-to-use, bottle volume 500 mL , filling volume
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About This Item
UNSPSC Code:
41106214
Recommended Products
agency
EP 2.6.1
JP 4.06
USP 71
71
Quality Level
sterility
sterile; autoclaved
form
liquid
feature
closure type crimp cap with septum
ready-to-use
packaging
bottle of
bottle capacity
500 mL
bottle volume
500 mL , filling volume
pH
7.1±0.2
application(s)
cosmetics
food and beverages
pharmaceutical
sterility testing
components
tween (1%)
storage temp.
2-25°C
suitability
nonselective for
General description
Fluid Thioglycollate Medium also known as FTM is a nutrient rich complex medium designed to serve as a sterility control for pharmaceutical products.
The presence of Thioglycollate and L-Cystine in the medium reduces the redox potential of the medium to create an anaerobic atmosphere. Additionally, 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.
The presence of Thioglycollate and L-Cystine in the medium reduces the redox potential of the medium to create an anaerobic atmosphere. Additionally, 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.
Application
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.
Fluid Thioglycollate Medium is recommended for sterility testing of samples according to EU and US pharmacopeia.
Features and Benefits
- 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.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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