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Quality Segment
agency
BP, ChP, JP, Ph. Eur., USP
description
EMPROVE® EXPERT Ph Eur,BP,USP,JP
product line
EMPROVE® EXPERT
potency
4220 mg/kg LD50, oral (Rat)
technique(s)
pH adjustment: suitable
pH
8.6 (20 °C, 50 g/L in H2O)
pKa (25 °C)
(1) 6.37, (2) 10.25 (carbonic acid)
mp
270 °C (decomposition)
density
2.22 g/cm3 at 20 °C, 2.16 g/mL at 25 °C (lit.)
bulk density
1000 kg/m3
application(s)
downstream processes
downstream processes
liquid formulation
liquid formulation
parenterals
pharma/biopharma processes
pharma/biopharma processes
upstream processes
storage temp.
2-30°C
SMILES string
[Na+].OC([O-])=O
InChI
1S/CH2O3.Na/c2-1(3)4;/h(H2,2,3,4);/q;+1/p-1
InChI key
UIIMBOGNXHQVGW-UHFFFAOYSA-M
General description
M-Clarity Program
As part of our EMPROVE® Program, our raw materials are offered with EMPROVE® Dossiers which provide comprehensive, up-to-date documentation to help you navigate regulatory challenges, manage risks, and improve your manufacturing processes.
Buffer quality is vital for the success of biopharmaceutical processes, because buffers are indispensable in nearly every production step.
Our broad portfolio of buffer materials manufactured under appropriate controls is tailored to your needs. Ranging from non-GMP grades for low-risk application, to IPEC-PQG GMP for higher-risk applications, we have products covering all your manufacturing needs.
Legal Information
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闪点 (F)
Not applicable
闪点 (°C)
Not applicable
存储类别
11 - Combustible Solids
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