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Opticap XLT20 Viresolve NFR 1-1/2 in. TC/TC

Name: Opticap XLT20 Viresolve NFR 1-1/2 in. TC/TC
Brand: MM

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About This Item

UNSPSC代码:

23151806

eCl@ss:

32031690

物料

polyethersulfone
polypropylene
polypropylene support
polypropylene vent cap
silicone seal

质量水平

400

描述

T-line with 1-1/2 in. Gauge Port

参数

≤32 mL/min air diffusion at 3.45 bar (50 psig) (in water)
25 °C max. inlet temp.
3.4 bar max. differential pressure (50 psid) (Reverse)
5.5 bar max. differential pressure (80 psid) (Forward)
5.5 bar max. inlet pressure (80 psi) at 23 °C
80 psig max. inlet pressure

技术

protein purification: suitable

长度

63.5 cm (25 in.)

设备尺寸

20 in.

过滤面积

0.854 m²

滞留体积

325 mL

入口接头直径

1 1/2 in.

outlet W

15.2 cm (6.0 in.)

出口接头直径

1-1/2 in.

尺寸

1200-2400 L

杂质

≤0.5 EU/mL Aqueous extraction (LAL test)

基质

Viresolve^® NFR

配件

1/4 in. hose barb (double O-ring Seal)
inlet sanitary flange
outlet sanitary flange
38 mm (1 1/2 in.) sanitary flange drain/vent

适用性

suitable for endotoxin

一般描述

A sample aqueous extraction contains less than 0.5 EU/mL as determined by the Limulus Amebocyte Lysate (LAL) test.

After wetting, may be autoclaved for 3 cycles of up to 60 min at 125 °C, using liquid cycle, slow exhaust.

包装

Double Easy-Open bag

分析说明

The extractables level was equal to or less than 70 mg after a 10 minute 1.5 LPM/ft² flush and 24 hours in water at controlled room temperature.

Will meet the USP Oxidizable Substances Test requirements after a water flush of ≥8 L

其他说明

EMD Millipore Corporation certifies that this product complies with the European Pressure Equipment Directive, 97/23/EC of 29 May 1997. This product has been classified under Article 3 § 3 of the Pressure Vessel Directive. It has been designed and manufactured in accordance with sound engineering practice to ensure safe use. In compliance with Article 3 § 3 of this Pressure Vessel Directive, this product does not bear the CE mark.

法律信息

VIRESOLVE is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

These products are manufactured in a facility which adheres to FDA Good Manufacturing Practices.

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