1.46631

Fluid Thioglycollate Medium with Neutralizers

Tween^® 0.1 %, bottle capacity 500 mL, bottle filling volume 500 mL, closure type, red flip cap with septum, pack of 6 bottles

• Synonym(e): FTM, Fluid Thioglycollate Medium, Thioglycollate Medium
• UNSPSC Code: 41106214
• NACRES: NA.72
• Bottle capacity: 500 mL
• Bottle filling volume: 500 mL
• Feature: closure type red flip cap with septum, ready-to-use
• Agency: EP 2.6.1, JP 4.06, USP 71
• Ph: 6.9-7.3

Eigenschaften

• Quality Segment: 300
• material: glass bottle
• agency: EP 2.6.1, JP 4.06, USP 71
• sterility: sterile; autoclaved (tested for 14 days at 30-35°C)
• form: liquid
• shelf life: 360 days
• feature: closure type red flip cap with septum, ready-to-use
• composition: Agar, 0.75 g , L-Cystine, 0.5 g , Glucose x H₂O, 5.5 g , NaCl, 2.5 g , Pancreatic Digest of Casein, 15 g , Resazurin: 1 mg, 1 mg , Sodium Thioglycollate, 0.5 g , Tween^®, 0.1% , Yeast Extract, 5 g
• packaging: pack of 6 bottles
• bottle capacity: 500 mL
• bottle filling volume: 500 mL
• pH: 6.9-7.3
• application(s): cosmetics; food and beverages; pharmaceutical; sterility testing
• storage temp.: 2-25°C
• suitability: nonselective for

Beschreibung

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.

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.

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.

Other Notes

Production will take place at Millipore SAS in Molsheim, France. Deliveries will be executed in accordance with the terms and conditions of MLS RTU GmbH. A minimum order quantity is required to process the order. Once the order is placed and confirmed, Merck will ensure product delivery within a maximum timeframe of 10 to 12 weeks. The terms and conditions of Merck KGaA apply to both Millipore SAS and MLS RTU GmbH and can be accessed through the following link: Standard Terms & Conditions

This medium can be modified and/or supplemented based on the required performance criteria.

Legal Information

TWEEN is a registered trademark of Croda International PLC

Disclaimer

This item is created at the customer′s request as a customized product and will not be developed or qualified in accordance with the Merck Product Development Process.

Sicherheitshinweise

• Lagerklasse: 12 - Non Combustible Liquids
• wgk: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable