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NACRES:
NA.74
UNSPSC Code:
41106200
Bottle capacity:
500 mL
Bottle filling volume:
500 mL
Feature:
closure type White screw cap with septum and protector, ready-to-use
Agency:
USP 71
Ph:
7.1 ( in H2O), 7.1
agency
USP 71
sterility
sterile; autoclaved
shelf life
12 mo.
feature
closure type White screw cap with septum and protector, ready-to-use
packaging
pkg of 500 mL, pack of 6 bottles
technique(s)
sterile filtration: suitable
bottle capacity
500 mL
bottle filling volume
500 mL
pH
7.1 ( in H2O), 7.1
Quality Level
application(s)
cosmetics
storage temp.
2-25°C
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General description
Fluid D is a washing solution for sterility testing of pharmaceutical samples containing lecithin or oil using the membrane filtration method. Rinse the membrane with Fluid D after filtration and provide a suitable medium to observe microbial growth.
Application
Fluid D is suitable for rinsing the solutions containing oil or lecithin during sterility testing by membrane filtration.
The oil should penetrate the membrane by its own weight followed by filtering applying the pressure or suction gradually. The membrane may be washed 3 times with 100 ml Fluid D (Fluid A with 0.1% Tween® 80) afterwards. At least one or one half of the filter is incubated in Tryptic Soy Broth (e.g. article number 146458) and a second or the other half of the filter in Fluid Thioglycollate Medium (e.g. article number 146385) for not less than 14 days.
The oil should penetrate the membrane by its own weight followed by filtering applying the pressure or suction gradually. The membrane may be washed 3 times with 100 ml Fluid D (Fluid A with 0.1% Tween® 80) afterwards. At least one or one half of the filter is incubated in Tryptic Soy Broth (e.g. article number 146458) and a second or the other half of the filter in Fluid Thioglycollate Medium (e.g. article number 146385) for not less than 14 days.
Features and Benefits
Our ready-to-use media provide the highest level of quality and testing confidence. They have been 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.
Legal Information
TWEEN is a registered trademark of Croda International PLC
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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