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Pentaethyleneglycol. Group: Biochemicals. Grades: Highly Purified. CAS No. 4792-15-8. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C10H22O6. US Biological Life Sciences.
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Pentaethyleneglycol
Pentaethyleneglycol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 4792-15-8. Pack Sizes: 1 g; 5 g. Product ID: HY-W007341.
PentaethyleneGlycol
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. in addition to pegylation, activated peg derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Alcohols. Alternative Names: 3,6,9,12-Tetraoxatetradecane-1,14-Diol. CAS No. 4792-15-8. Molecular formula: C10H22O6. Mole weight: 238.28. Purity: 0.98. IUPACName: 2-[2-[2-[2- (2-hydroxyethoxy) ethoxy]ethoxy]ethoxy]ethanol. Canonical SMILE
PentaethyleneGlycol
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated peg derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. pegylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of peg improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and redu. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. Alternative Names: 3,6,9,12-Tetraoxatetradecane-1,14-Diol. CAS No. 4792-15-8. Product ID: 2-[2-[2-[2- (2-hydroxyethoxy) ethoxy]ethoxy]ethoxy]ethanol. Molecular formula: 238.28. Mole weight: C10H22O6. C(COCCOCCOCCOCCO)O. 1S / C10H22O6 / c11-1-3-13-5-7-15-9-10-16-8-6-14-4-2- 12 / h11-12H, 1-10H2. JLFNLZLINWHATN-UHFFFAOYSA-N. 98%.
Intermediate in the production of alkylating agents. Group: Biochemicals. Alternative Names: 3,6,9,12-Tetraoxatetradecane-1,14-diol 1,14-Dimethanesulfonate; PentaethyleneGlycol Dimesylate. Grades: Highly Purified. CAS No. 109789-39-1. Pack Sizes: 500mg. US Biological Life Sciences.
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PentaethyleneGlycol Dodecyl Ether
Heterocyclic Organic Compound. CAS No. 003055-95-6. Purity: N/A. Catalog: ACM003055956.
Pentaethyleneglycol monomethyl ether is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 23778-52-1. Pack Sizes: 5 g; 25 g; 100 g. Product ID: HY-W042713.
2,5,8,11,14,17-Hexaoxaoctadecane, a derivative of polyethylene glycol (PEG), has become a ubiquitous solubilizer and carrier in the biomedicine industry. Widely utilized for its efficacy in drug delivery, it facilitates the targeted treatment of malignant neoplasms, HIV, and neurodegenerative diseases such as Alzheimer's, amongst others. Its implications continue to yield promising results in the field of contemporary medical research. Synonyms: Pentaethyleneglycol dimethyl ether; 1,14-dimethoxy-3,6,9,12-tetraoxa-tetradecane; NSC 244990; 1,2-bis-[2-2-Methoxy-ethoxy-ethoxy]-ethane; O,O'-Dimethyl-pentaethyleneglycol; Pentaglyme. Grades: 95%. CAS No. 1191-87-3. Molecular formula: C12H26O6. Mole weight: 266.33.
n-Octylpentaoxyethylene
n-Octylpentaoxyethylene. Group: Biochemicals. Alternative Names: Pentaethyleneglycol monooctylether. Grades: Highly Purified. CAS No. 19327-40-3. Pack Sizes: 500mg, 1g, 2g, 5g. US Biological Life Sciences.
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