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经验公式(希尔记法):
C10H17N3O6S
化学文摘社编号:
分子量:
307.32
UNSPSC Code:
12352209
EC Index Number:
200-725-4
MDL number:
产品名称
谷胱甘肽(还原型), suitable for biopharmaceutical production EMPROVE® bio Ph Eur
SMILES string
SCC(NC(=O)CCC([N+H3])C(=O)[O-])C(=O)NCC(=O)O
InChI
1S/C10H17N3O6S/c11-5(10(18)19)1-2-7(14)13-6(4-20)9(17)12-3-8(15)16/h5-6,20H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)
InChI key
RWSXRVCMGQZWBV-UHFFFAOYSA-N
agency
Ph. Eur.
pH
3 (20 °C, 10 g/L in H2O)
mp
185-195 °C
solubility
100 g/L
bulk density
160 kg/m3
storage temp.
2-8°C
Quality Level
product line
EMPROVE® EXPERT
application(s)
pharma/biopharma processes
Analysis Note
Assay (iodometric, calc. on dried substance): 98.0 - 101.0 %
Identity (IR-spectrum): passes test
Appearance: white to almost white, slightly agglomerated, crystalline powder
Appearance of solution (100 g/l, water): clear and colorless.
Spec. rotation (α 20/D, 40 g/l, water, calc. on dried substance): -15.5° to -17.5°
Chloride (Cl): ≤ 200 ppm
Sulfate (SO₄): ≤ 300 ppm
As (Arsenic): ≤ 1.5 ppm
Fe (Iron): ≤ 10 ppm
Fe (Iron) (ICP): ≤ 10 ppm
NH₄ (Ammonium): ≤ 200 ppm
Cu (Copper)*: ≤ 25 ppm
Related substances (CE) (Impurity A (Cysteinylglycine)): ≤ 0.5 %
Related substances (CE) (Impurity B (Cysteine)): ≤ 0.5 %
Related substances (CE) (Impurity C (Glutathione oxidized)): ≤ 1.5 %
Related substances (CE) (Impurity D (Glutamylcysteine)): ≤ 1.0 %
Related substances (CE) (Impurity E): ≤ 0.5 %
Related substances (CE) (Largest unspecified impurity): ≤ 0.2 %
Related substances (CE) (Sum of all impurities): ≤ 2.5 %
Acetic acid (HS-GC): ≤ 5000 ppm
Ethanol (HS-GC): ≤ 5000 ppm
Ethyl acetate (HS-GC): ≤ 5000 ppm
Other residual solvents (ICH Q3C): passes test
Sulfated ash (600 °C): ≤ 0.1 %
Loss on drying (105 °C; 3 h): ≤ 0.5 %
Elemental impurity specifications have been set considering ICH Q3D (Guideline for Elemental Impurities). Class 1-3 elements are not likely to be present above the ICH Q3D option 1 limit, unless specified and indicated (*).
Corresponds to Ph. Eur.
Identity (IR-spectrum): passes test
Appearance: white to almost white, slightly agglomerated, crystalline powder
Appearance of solution (100 g/l, water): clear and colorless.
Spec. rotation (α 20/D, 40 g/l, water, calc. on dried substance): -15.5° to -17.5°
Chloride (Cl): ≤ 200 ppm
Sulfate (SO₄): ≤ 300 ppm
As (Arsenic): ≤ 1.5 ppm
Fe (Iron): ≤ 10 ppm
Fe (Iron) (ICP): ≤ 10 ppm
NH₄ (Ammonium): ≤ 200 ppm
Cu (Copper)*: ≤ 25 ppm
Related substances (CE) (Impurity A (Cysteinylglycine)): ≤ 0.5 %
Related substances (CE) (Impurity B (Cysteine)): ≤ 0.5 %
Related substances (CE) (Impurity C (Glutathione oxidized)): ≤ 1.5 %
Related substances (CE) (Impurity D (Glutamylcysteine)): ≤ 1.0 %
Related substances (CE) (Impurity E): ≤ 0.5 %
Related substances (CE) (Largest unspecified impurity): ≤ 0.2 %
Related substances (CE) (Sum of all impurities): ≤ 2.5 %
Acetic acid (HS-GC): ≤ 5000 ppm
Ethanol (HS-GC): ≤ 5000 ppm
Ethyl acetate (HS-GC): ≤ 5000 ppm
Other residual solvents (ICH Q3C): passes test
Sulfated ash (600 °C): ≤ 0.1 %
Loss on drying (105 °C; 3 h): ≤ 0.5 %
Elemental impurity specifications have been set considering ICH Q3D (Guideline for Elemental Impurities). Class 1-3 elements are not likely to be present above the ICH Q3D option 1 limit, unless specified and indicated (*).
Corresponds to Ph. Eur.
General description
Our SAFC® portfolio of high-quality products for biopharmaceutical processing withstands strict quality control procedures and is produced according to MQ-500 requirements as defined by the M-Clarity program.
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.
Our comprehensive portfolio of downstream process chemicals not only provides biopharmaceutical manufacturers with high-quality raw materials for production of classical and novel therapies, but also helps them get to market faster and simplify regulatory challenges. 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.
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.
Our comprehensive portfolio of downstream process chemicals not only provides biopharmaceutical manufacturers with high-quality raw materials for production of classical and novel therapies, but also helps them get to market faster and simplify regulatory challenges. 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
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFC is a registered trademark of Merck KGaA, Darmstadt, Germany
Application
Glutathione (reduced) is essential in biopharmaceutical manufacturing, serving as a powerful antioxidant that protects cells and proteins from oxidative damage. It maintains a favorable redox environment, enhancing protein folding and stability, which is vital for the efficacy of therapeutic proteins. Additionally, glutathione (reduced) supports cellular health and viability in mammalian cell cultures, leading to improved yields and productivity in the production of biologics. Overall, it plays a critical role in ensuring the integrity and quality of final pharmaceutical products.
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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