8.17061
Tween® 80 (polysorbate)
EMPROVE® ESSENTIAL, Ph. Eur., JP, NF
Fabrication pharma
Synonyme(s) :
TWEEN® 80, Mono-oléate de polyoxy-éthylènesorbitane, Mono-oléate de polyéthylène glycol sorbitane, Monooléate de POE (20)-sorbitane, Polysorbate 80
About This Item
Produits recommandés
Agence
JP
NF
Ph. Eur.
Niveau de qualité
Pression de vapeur
<1.33 hPa
Gamme de produits
EMPROVE® ESSENTIAL
Forme
viscous liquid
Technique(s)
API processing | nano-milling: suitable
pH
5-7 (20 °C, 50 g/L in H2O)
kinematic viscosity
300-500 cSt(25 °C)
Point d'ébullition
>100 °C/1013 hPa
Température de transition
flash point >149 °C
Densité
1.07 g/cm3 at 25 °C
Application(s)
liquid formulation
ophthalmics
pharma/biopharma processes
pharmaceutical
semi-solid formulation
solid formulation
solubility enhancement
Température de stockage
15-25°C
Chaîne SMILES
CCCCCCCC/C=C/CCCCCCCC(=O)OCCOCC(C1C(CC(O1)OCCO)OCCO)OCCO
InChI
1S/C32H60O10/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-30(36)40-25-24-37-27-29(39-22-19-34)32-28(38-21-18-33)26-31(42-32)41-23-20-35/h9-10,28-29,31-35H,2-8,11-27H2,1H3/b10-9+
Clé InChI
RGPBUVUVZKQNHD-MDZDMXLPSA-N
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Description générale
Dans le cadre de notre programme Emprove®, nos matières premières sont accompagnées d'une documentation complète qui permet d'assurer la conformité de votre produit pharmaceutique ou biopharmaceutique, la parfaite transparence de votre chaîne d'approvisionnement et l'atténuation des risques. Notre marque SAFC® est une famille de produits de haute qualité, pour la formulation et la production pharmaceutiques et biopharmaceutiques, qui satisfait aux procédures de contrôle qualité les plus strictes et qui est produite conformément aux bonnes pratiques de fabrication en vigueur.
Application
Informations légales
Application
Produit(s) apparenté(s)
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
>235.4 °F - closed cup
Point d'éclair (°C)
> 113 °C - closed cup
Certificats d'analyse (COA)
Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".
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Medicine for children poses unique formulation challenges compared to adults. Consider developmental physiology and age specifics when designing pharmaceuticals. Quality issues can severely impact patient safety. Therefore, excipient quality, supplier selection, and supply chain security are crucial, particularly for pediatric formulations.
Medicine for children poses unique formulation challenges compared to adults. Consider developmental physiology and age specifics when designing pharmaceuticals. Quality issues can severely impact patient safety. Therefore, excipient quality, supplier selection, and supply chain security are crucial, particularly for pediatric formulations.
Medicine for children poses unique formulation challenges compared to adults. Consider developmental physiology and age specifics when designing pharmaceuticals. Quality issues can severely impact patient safety. Therefore, excipient quality, supplier selection, and supply chain security are crucial, particularly for pediatric formulations.
Medicine for children poses unique formulation challenges compared to adults. Consider developmental physiology and age specifics when designing pharmaceuticals. Quality issues can severely impact patient safety. Therefore, excipient quality, supplier selection, and supply chain security are crucial, particularly for pediatric formulations.
Contenu apparenté
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
This page summarizes key considerations related to regulatory expectations for biomanufacturing including chemicals and polymeric materials. For chemicals, topics include nitrosamines and elemental impurities, and for polymeric materials such as filters and single-use assemblies, the focus is qualification and extractable and leachable testing.
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