1.08212
Parteck® PLX 188 (Poloxamer 188)
(stabilized with 70ppm BHT), EMPROVE® ESSENTIAL, Ph. Eur., ChP, NF
別名:
Poloxamer 188
製品名
Parteck® PLX 188 (Poloxamer 188), (stabilized with 70ppm BHT), EMPROVE® ESSENTIAL, Ph. Eur., ChP, NF
SMILES string
O2C(C2)C.O1CC1
InChI
1S/C3H6O.C2H4O/c1-3-2-4-3;1-2-3-1/h3H,2H2,1H3;1-2H2
InChI key
RVGRUAULSDPKGF-UHFFFAOYSA-N
biological source
synthetic
agency
ChP
NF
Ph. Eur.
product line
EMPROVE® ESSENTIAL
bp
>150 °C
mp
55 °C
bulk density
1050 kg/m3
storage temp.
2-25°C
Quality Level
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Application
Parteck® PLX 188 excipient combines adequate lubrication at tolerable concentrations with the added benefit of dissolution enhancement. It features consistent performance, improved dissolution rate and reliable lubrication – all at the same time. As a result, Parteck® PLX 188 excipient can therefore provide a simple solution to low bioavailability of DCS 2a compounds.
Features and Benefits
- Hydrophilic, water-soluble tablet lubrication
- Improved dissolution rates for poorly soluble DCS class IIa molecules
- Specified particle size distribution optimized for solid application performance
- Regulatory support through compliance with Ph. Eur. and USP-NF, going beyond current requirements with specitied formaldehyde content
General description
With formulation challenges in mind, we have used particle engineering technologies to develop functional excipients specifically for solid oral dosage forms. The products in our Parteck® portfolio feature unique particle properties tailored for excellent performance in tableting processes, for specific drug delivery technologies, or for solubility enhancement.
As part of our Emprove® Program, our raw materials are offered with extensive documentation facilitating compliance of your pharma and biopharma product, full supply chain transparency and risk mitigation. Our SAFC® portfolio of high-quality products for biopharmaceutical and pharmaceutical formulation and production withstands strict quality control procedures and is produced according to applicable cGMP guidelines.
As part of our Emprove® Program, our raw materials are offered with extensive documentation facilitating compliance of your pharma and biopharma product, full supply chain transparency and risk mitigation. Our SAFC® portfolio of high-quality products for biopharmaceutical and pharmaceutical formulation and production withstands strict quality control procedures and is produced according to applicable cGMP guidelines.
Legal Information
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
PARTECK is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFC is a registered trademark of Merck KGaA, Darmstadt, Germany
保管分類
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
資料
Our overview of API solubility and dissolution enhancement methods can help you decide between the many options to take during formulation.
関連コンテンツ
グローバルトレードアイテム番号
| カタログ番号 | GTIN |
|---|---|
| 1.08212.9025 | 04061841048671 |
| 1.08212.0500 | 04061841048657 |
| 1.08212.0001 | 04061841048640 |
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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