Alfa Chemistry Materials 5 - Products
Alfa Chemistry Materials is specialized in material chemistry and offers an extensive catalog of materials in a wide range of applications, including Metals and Materials, 3D Printing Materials, Biomaterials.
| Product | Description | |
|---|---|---|
| Polyester bis-MPA dendron, 32 hydroxyl, 1 amine | Polyester dendritic structures which are based on 2,2-bismethylolpropionic acid (bis-MPA) monomer are highly branched and can be end functionalized with a wide range of functional groups. They are widely used in biosensors, optics, adhesives and coatings. The hydroxyl and amine end surface groups increase the biocompatibility and the scaffolding ability of these dendritic polymers. Uses: Amine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination. Group: Dendrimers. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 5. |  |
| Polyester bis-MPA dendron, 32 hydroxyl, 1 azide | Calculated mol. wt. 3742.8. Uses: Azide dendrons can be coupled to acetylene functionalized molecules, including acetylene dendrons to form asymmetric dendrimers. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 5. | |
| Polyester bis-MPA dendron, 32 hydroxyl, 1 thiol | calculated mol. wt. 3677.7. Uses: Thiol dendrons can be conjugated to varius noble surfaces or coupled to unsaturated carbon-carbon bonds using various radical initiators. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 5. | |
| Polyester bis-MPA dendron, 4 hydroxyl, 1 acetylene | calculated mol. wt. 404.4. Uses: Acetylene dendrons can be coupled to azide functional molecules such as carbohydrates, fluorescent dyes and polymers. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. CAS No. 1055361-96-0. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 2. CC (CO) (CO)C (=O)OCC (C) (COC (=O)C (C) (CO)CO)C (=O)OCC#C. 1S/C18H28O10/c1-5-6-26-15(25)18(4, 11-27-13(23)16(2, 7-19)8-20)12-28-14(24)17(3, 9-21)10-22/h1, 19-22H, 6-12H2, 2-4H3. OENNSQAEPFFGAD-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 4 hydroxyl, 1 azide | Dendrimers and dendrons are symmetrically branched polymer structures that possess a well-defined spatial distribution of functional groups. The properties of dendrimers are steered by controlling the generation number, repeating unit, end groups. hydrophilicity/hydrophobicity are controlled by the functionality of the end groups. Uses: These form extremely attractive molecular targets. nanotechnological applications range from microelectronics to biomedical devices.2 other proposed applications are: coatings resins additives, analytical techniques medicine drug and dye delivery molecular imprinting organic polymer synthesis catalysis optoelectronic applications. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. CAS No. 919988-18-4. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 2. CC (CO) (CO)C (=O)OCC (C) (COC (=O)C (C) (CO)CO)C (=O)OCCCCCCN=[N+]=[N-]. 1S/C21H37N3O10/c1-19 (10-25, 11-26)16 (29)33-14-21 (3, 15-34-17 (30)20 (2, 12-27)13-28)18 (31)32-9-7-5-4-6-8-23-24-22/h25-28H, 4-15H2, 1-3H3. LGPUUVBKCMNFLE-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 8 carboxyl, 1 amine | We offer a diverse selection of dendrimers containing a large number of peripheral groups. Uses: Amine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 3. 1S/C75H99NO46/c1-8-75 (41-116-62 (101)44-9-11-45 (76)12-10-44, 42-121-67 (106)73 (6, 37-117-63 (102)69 (2, 29-108-54 (93)21-13-46 (77)78)30-109-55 (94)22-14-47 (79)80)38-118-64 (103)70 (3, 31-110-56 (95)23-15-48 (81)82)32-111-57 (96)24-16-49 (83)84)43-122-68 (107)74 (7, 39-119-65 (104)71 (4, 33-112-58 (97)25-17-50 (85)86)34-113-59 (98)26-18-51 (87)88)40-120-66 (105)72 (5, 35-114-60 (99)27-19-52 (89)90)36-115-61 (100)28-20-53 (91)92/h9-12H, 8, 13-43, 76H2, 1-7H3, (H, 77, 78) (H, 79, 80) (H, 81, 82) (H, 83, 84) (H, 85, 86) (H, 87, 88) (H, 89, 90) (H, 91, 92). ACOBVJDQVWUHRD-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 8 hydroxyl, 1 allyl | calculated mol. wt. 870.9. Uses: Allyl dendrons can be coupled to thiol functional molecules. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. CAS No. 1282509-84-5. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 3. CC (CO) (CO)C (=O)OCC (C) (COC (=O)C (C) (CO)CO)C (=O)OCC (C) (COC (=O)C (C) (COC (=O)C (C) (CO)CO)COC (=O)C (C) (CO)CO)C (=O)OCC=C. 1S/C38H62O22/c1-9-10-54-29(51)36(6, 19-59-30(52)37(7, 21-55-25(47)32(2, 11-39)12-40)22-56-26(48)33(3, 13-41)14-42)20-60-31(53)38(8, 23-57-27(49)34(4, 15-43)16-44)24-58-28(50)35(5, 17-45)18-46/h9, 39-46H, 1, 10-24H2, 2-8H3. KBDYZZKBEBTIML-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 8 hydroxyl, 1 amine | calculated mol. wt. 950. Uses: Amine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 3. CCC (COC (=O)c1ccc (N)cc1) (COC (=O)C (C) (COC (=O)C (C) (CO)CO)COC (=O)C (C) (CO)CO)COC (=O)C (C) (COC (=O)C (C) (CO)CO)COC (=O)C (C) (CO)CO. 1S/C43H67NO22/c1-8-43 (25-60-30 (53)28-9-11-29 (44)12-10-28, 26-65-35 (58)41 (6, 21-61-31 (54)37 (2, 13-45)14-46)22-62-32 (55)38 (3, 15-47)16-48)27-66-36 (59)42 (7, 23-63-33 (56)39 (4, 17-49)18-50)24-64-34 (57)40 (5, 19-51)20-52/h9-12, 45-52H, 8, 13-27, 44H2, 1-7H3. ABFRDJWLXWYYKC-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 8 hydroxyl, 1 azide | calculated mol. wt. 956. Uses: Azide dendrons can be coupled to acetylene functionalized molecules, including acetylene dendrons to form asymmetric dendrimers. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. CAS No. 873849-89-9. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 3. CC (CO) (CO)C (=O)OCC (C) (COC (=O)C (C) (CO)CO)C (=O)OCC (C) (COC (=O)C (C) (COC (=O)C (C) (CO)CO)COC (=O)C (C) (CO)CO)C (=O)OCCCCCCN=[N+]=[N-]. 1S/C41H69N3O22/c1-35 (14-45, 15-46) 28 (53) 61-24-40 (6, 25-62-29 (54) 36 (2, 16-47) 17-48) 33 (58) 65-22-39 (5, 32 (57) 60-13-11-9-8-10-12-43-44-42) 23-66-34 (59) 41 (7, 26-63-30 (55) 37 (3, 18-49) 19-50) 27-64-31 (56) 38 (4, 20-51) 21-52/h45-52H, 8-27H2, 1-7H3. RHUOETMPCLTKIU-UHFFFAOYSA-N. | |
| Polyester bis-MPA dendron, 8 hydroxyl, 1 thiol, generation 3 | calculated mol.wt.890.9. Uses: Thiol dendrons can be conjugated to varius noble surfaces or coupled to unsaturated carbon-carbon bonds using various radical initiators. Group: Dendrimers. Alternative Names: bisMPA dendrimer, bisMPA dendron. Pack Sizes: 250 mg in glass insert. Molecular formula: generation 3. CC (O) (O)C (=O)OCC (C) (COC (=O)C (C) (O)O)C (=O)OCC (C) (COC (=O)C (C) (COC (=O)C (C) (O)O)COC (=O)C (C) (O)O)C (=O)OCCS. 1S/C29H46O22S/c1-23(16(30)45-8-9-52, 10-46-17(31)24(2, 12-48-19(33)26(4, 37)38)13-49-20(34)27(5, 39)40)11-47-18(32)25(3, 14-50-21(35)28(6, 41)42)15-51-22(36)29(7, 43)44/h37-44, 52H, 8-15H2, 1-7H3. JKFYZSQKFIZEKR-UHFFFAOYSA-N. | |
| Poly(ethyl acrylate) solution | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Biocompatible pea based copolymer membranes may find several s such as keratoprosthesis. Group: Hydrophobic polymers. Alternative Names: Acrylic acid ethyl ester polymer, Ethyl acrylate homopolymer. CAS No. 9003-32-1. Pack Sizes: 50 g in glass bottle. Product ID: ethyl prop-2-enoate. Molecular formula: average Mw ~95,000 by GPC. Mole weight: CH2CHCOOC2H5;C5H8O2;C5H8O2. CCOC(=O)C=C. 1S/C5H8O2/c1-3-5(6)7-4-2/h3H, 1, 4H2, 2H3. JIGUQPWFLRLWPJ-UHFFFAOYSA-N. | |
| Poly(ethylene-alt-maleic anhydride) | The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Viscosity modifier for solution, suspension or emulsion. dispersing aid for insoluble solids. Group: Hydrophilic polymers. Alternative Names: maleic copolymer, maleated copolymer, maleated polymer. CAS No. 9006-26-2. Pack Sizes: Packaging 100, 500 g in poly bottle. Molecular formula: average Mw 100,000-500,000. 1S/C4H2O3.C2H4/c5-3-1-2-4(6)7-3; 1-2/h1-2H; 1-2H2. YYXLGGIKSIZHSF-UHFFFAOYSA-N. | |
| Polyethylene-block-poly(ethylene glycol) | We offer you this block copolymer with good biocompatibility. Uses: Nonionic surfactant. emulsifier for coatings, ceramics, metalworking fluids and inks. lubricant. mold release agent. thickening agent. nonionic surfactant. Group: Poly(ethylene glycol) and poly(ethylene oxide)self-assembly materials. Pack Sizes: 250 g in poly bottle. Molecular formula: average Mn ~1,400. Mole weight: CH3CH2(CH2CH2)X(OCH2CH2)YOH. C=C.OCCO. | |
| Poly(ethylene-co-acrylic acid) zinc salt | Poly(ethylene-co-acrylic acid) zinc salt. Group: Hydrophobic polymers. CAS No. 28208-80-2. Product ID: zinc; ethene; prop-2-enoate. Molecular formula: 235.5g/mol. Mole weight: C8H10O4Zn. C=C.C=CC(=O)[O-].C=CC(=O)[O-].[Zn+2]. InChI=1S/2C3H4O2. C2H4. Zn/c2*1-2-3(4)5; 1-2; /h2*2H, 1H2, (H, 4, 5); 1-2H2; /q; ; ; +2/p-2. HENHBQJZXRPLOX-UHFFFAOYSA-L. | |
| Poly(ethylene-co-ethyl acrylate) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymers. CAS No. 9010-86-0. Product ID: ethene; ethyl prop-2-enoate. Molecular formula: 128.17g/mol. Mole weight: (CH2CH2)x[CH2CH(CO2C2H5)]y. C=C.CCOC(=O)C=C. 1S/C5H8O2.C2H4/c1-3-5(6)7-4-2; 1-2/h3H, 1, 4H2, 2H3; 1-2H2. CGPRUXZTHGTMKW-UHFFFAOYSA-N. | |
| Poly(ethylene-co-propylene-co-5-methylene-2-norbornene) | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Our hydrophobic polymers are used as coatings, adhesives, fibers, films and engineering plastics. furthermore, they are widely used as biomedical polymers for vascular grafts, implants and ophthalmic applications. Group: Hydrophobic polymers. Alternative Names: Ethylene-ethylidenenorbornene-propylene copolymer. CAS No. 25038-36-2. 1S/C9H12. C3H6. C2H4/c1-2-8-5-7-3-4-9(8)6-7; 1-3-2; 1-2/h2-4, 7, 9H, 5-6H2, 1H3; 3H, 1H2, 2H3; 1-2H2/b8-2+;. MPXNNMASLYQCAH-SZPWSVBHSA-N. | |
| Poly(ethylene-co-vinyl acetate) | Poly(ethylene-co-vinyl acetate). Group: Hydrophobic polymerspolymers. CAS No. 24937-78-8. Product ID: ethene; ethenyl acetate. Molecular formula: 114.14g/mol. Mole weight: C6H10O2. CC(=O)OC=C.C=C. InChI=1S/C4H6O2.C2H4/c1-3-6-4(2)5; 1-2/h3H, 1H2, 2H3; 1-2H2. HDERJYVLTPVNRI-UHFFFAOYSA-N. | |
| Poly(ethylene glycol), 16 acetylene dendron, generation 3 | Dendrimers and dendrons are symmetrically branched polymer structures that possess a well-defined spatial distribution of functional groups. Dendrimers are chemically modified by attaching poly ethylene glycol (PEG) molecule to increase its solubility and prolong circulation half-life."Clickable groups", such as primary acetylenes, are introduced to the mono dispersed dendritic structures, using "click" chemistry. These acetylene groups, attached to Bis-MPA based dendrons, allow it to form the conjugates with bioactive moieties such as carbohydrate, fluorescent dyes, disaccharides etc. Uses: The proposed uses are: as an efficient drug delivery system. in vitro toxicological studies; in vivo via radionuclide labeling and optical imaging biosensors;dip pen nanolithography. Group: Dendrimers. Alternative Names: PFD-G3-PEG6k-Acetylene, Dendron functionalized PEG acetylene, generation 3, Bis[2,2-bis(hydroxymethyl)propanoic acid] PEG, PEG-6000, Bis-MPA poly(ethylene glycol). Pack Sizes: Packaging 500 mg in glass insert. Molecular formula: PEG average Mn 6000 (n~130, esterified with 16 acetylene groups) Mn 7500-9500 (by NMR) average Mn 8000. | |
| Poly(ethylene glycol), 16 hydroxyl dendron, generation 3 | Poly(ethylene glycol), 16 hydroxyl dendron, generation 3. Group: Poly(ethylene glycol) and poly(ethylene oxide)dendrimers. | |
| Poly(ethylene glycol) 2-aminoethyl ether acetic acid | Poly(ethylene glycol) 2-aminoethyl ether acetic acid. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 139729-28-5. | |
| Poly(ethylene glycol) 2-aminoethyl ether acetic acid | 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: Bioconjugation drug discovery. Group: Poly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG average Mn 5000 (n~110) average Mn 5000. | |
| Poly(ethylene glycol) 2-aminoethyl ether biotin | 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: Bioconjugation, drug delivery, peg hydrogel, crosslinker, surface functionalization. Group: Poly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG average Mn 3,400 (n~77). | |
| Poly(ethylene glycol), 32 hydroxyl dendron, generation 4 | Poly(ethylene glycol), 32 hydroxyl dendron, generation 4. Group: Dendrimers. | |
| Poly(ethylene glycol), 4 acetylene dendron, generation 1 | Poly(ethylene glycol), 4 acetylene dendron, generation 1. Group: Dendrimers. | |
| Poly(ethylene glycol) 4-cyano-4-(phenylcarbonothioylthio)pentanoate | Poly(ethylene glycol) 4-cyano-4-(phenylcarbonothioylthio)pentanoate. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol), 4 hydroxyl dendron, generation 1 | Poly(ethylene glycol), 4 hydroxyl dendron, generation 1. Group: Poly(ethylene glycol) and poly(ethylene oxide)dendrimers. | |
| Poly(ethylene glycol) 4-nonylphenyl 3-sulfopropyl ether potassium salt | Poly(ethylene glycol) 4-nonylphenyl 3-sulfopropyl ether potassium salt. Group: Self-assembly materials. CAS No. 119438-10-7. Molecular formula: 1260.0. Mole weight: C58H109KO24S. Technical grade. | |
| Poly(ethylene glycol), 8 acetylene dendron, generation 2 | Poly(ethylene glycol), 8 acetylene dendron, generation 2. Group: Dendrimers. | |
| Poly(ethylene glycol), 8 hydroxyl dendron, generation 2 | Poly(ethylene glycol), 8 hydroxyl dendron, generation 2. Group: Poly(ethylene glycol) and poly(ethylene oxide)dendrimers. CAS No. 352708-21-5. | |
| Poly(ethylene glycol) α-hydroxy-ω-azido terminated | Poly(ethylene glycol) α-hydroxy-ω-azido terminated. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol), α -maleimidopropionamide-ω -formyl terminated | 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: Difunctionalized peg used for protein attachment. Group: Poly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: Packaging 250 mg in glass insert. Molecular formula: average Mn 3000. | |
| Poly(ethylene glycol) bis(2-bromoisobutyrate) | Poly(ethylene glycol) bis(2-bromoisobutyrate). Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol) bis(2-bromoisobutyrate) | 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: Peg functionalized with bromoisobutyryl group to initiate atom transfer radical polymerization (atrp). this macroinitiator can be used to increase biocompatibility; hydrophilicity; or generate a triblock copolymer with peg as the middle block. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-ATRP, PEG-Bib, Dibromoisobutyryl PEG. CAS No. 467254-02-0. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: PEG average Mn 300 (n ~ 7) average Mn 700. | |
| Poly(ethylene glycol) bis(3-aminopropyl) terminated | 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). Alternative Names: O,O'-Bis(3-aminopropyl)polyethylene glycol 1,500. CAS No. 34901-14-9. Molecular formula: Mn ~1,500. OCCO.NCCCO. 1S/C3H9NO.C2H6O2/c4-2-1-3-5; 3-1-2-4/h5H, 1-4H2; 3-4H, 1-2H2. ZEXFKFYUMFXUBE-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) bis(amine) | Poly(ethylene glycol) bis(amine). Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 24991-53-5. | |
| Poly(ethylene glycol) bisazide | 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: Peg functionalized with azide for ligation and coupling reactions. this can also be crosslinked into hydrogels. Group: Poly(ethylene glycol) and poly(ethylene oxide). Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: PEG average Mn 10000 (n~230) average Mn 10000. | |
| Poly(ethylene glycol) bisazide | Poly(ethylene glycol) bisazide. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 82055-94-5. | |
| Poly(ethylene glycol) bis(carboxymethyl) ether | Poly(ethylene glycol) bis(carboxymethyl) ether. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Polyoxyethylene bis(acetic acid). CAS No. 39927-08-7. Product ID: Ethane-1,2-diol; 2-hydroxyacetic acid. Molecular formula: 138.12. Mole weight: C4H10O5. C(CO)O.C(C(=O)O)O. InChI=1S/C2H4O3.C2H6O2/c3-1-2(4)5; 3-1-2-4/h3H, 1H2, (H, 4, 5); 3-4H, 1-2H2. SZUIEBOFAKRNDS-UHFFFAOYSA-N. >90%. | |
| Poly(ethylene glycol)-block-polylactide methyl ether | Biodegradable, water-soluble polymer. Uses: Applications include drug encapsulation and drug delivery. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-b-PLA. Pack Sizes: 1 g in glass bottle. Molecular formula: PEG average Mn 750 PLA average Mn 1,000. Mole weight: CH3O(CH2CH2O)x(COCHCH3O)yH. | |
| Poly(ethylene glycol)-block-poly(N-isopropylacrylamide) | Poly(ethylene glycol)-b-poly(N-isopropylacrylamide) (PEG110-b-PNIPAM44) undergoes thermoresponsive micellization in water, forming micelles of varied size, structure and distribution depending on the concentration of the block copolymer. Uses: Well-defined peg-block-pnipam diblock copolymers can form thermoresponsive vesicles in water and enable controlled drug release. Group: Hydrophilic polymers. Alternative Names: PEGylated polyNIPAM, PEG-block-PNIPAM, PEG-b-polyNIPAM, PNIPAAm. Pack Sizes: 500 mg in glass bottle. Molecular formula: PEG Mn 2,000 PNIPAM Mn 24,000. Mole weight: CH3(OC2H4)mC6H7NO2(C6H11NO)nH. | |
| Poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) | Liquid. Group: Peg-ppg copolymerspoly(ethylene glycol) and poly(ethylene oxide)self-assembly materials. CAS No. 9003-11-6. Product ID: 2-methyloxirane; oxirane. Molecular formula: 102.13g/mol. Mole weight: C5H10O2. CC1CO1.C1CO1. InChI=1S/C3H6O.C2H4O/c1-3-2-4-3; 1-2-3-1/h3H, 2H2, 1H3; 1-2H2. RVGRUAULSDPKGF-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) diacetylene | 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: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG diacetylene, PEG bis(4-pentynoate)terminated, Poly(ethylene glycol) bis(4-pentynoate) terminated. Molecular formula: average Mn 2000. | |
| Poly(ethylene glycol) diacrylamide | 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: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 160556-48-9. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 3,700. | |
| Poly(ethylene glycol) diamine | Poly(ethylene glycol) diamine. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 24991-53-5. | |
| Poly(ethylene glycol) diglycidyl ether | Liquid. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 72207-80-8. Product ID: 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane. Molecular formula: 174.19g/mol. Mole weight: C8H14O4. C1C(O1)COCCOCC2CO2. InChI=1S/C8H14O4/c1 (9-3-7-5-11-7)2-10-4-8-6-12-8/h7-8H, 1-6H2. AOBIOSPNXBMOAT-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) dimethyl ether | 1,2-dimethoxyethane appears as a liquid with a sharp odor. Less dense than water. Flash point 34°F. Mildly toxic by ingestion and inhalation. Severely irritates skin and eyes. Vapors heavier than air. Used to make other chemicals.;Liquid;Liquid;COLOURLESS LIQUID WITH CHARACTERISTIC ODOUR. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 24991-55-7. Product ID: 1,2-dimethoxyethane. Molecular formula: 90.12g/mol. Mole weight: C4H10O2; CH3OCH2CH2OCH3; C4H10O2; C4H10O2. COCCOC. InChI=1S / C4H10O2 / c1-5-3-4-6-2 / h3-4H2, 1-2H3. XTHFKEDIFFGKHM-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) dithiol | Poly(ethylene glycol) dithiol. Group: Poly(ethylene glycol) and poly(ethylene oxide). Product ID: 2-(2-sulfanylethoxy)ethanethiol. Molecular formula: 138.3g/mol. Mole weight: C4H10OS2. C(CS)OCCS. InChI=1S / C4H10OS2 / c6-3-1-5-2-4-7 / h6-7H, 1-4H2. CNDCQWGRLNGNNO-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) ditosylate | 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: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG ditosylate. Molecular formula: average Mn 20000. | |
| Poly(ethylene glycol) divinyl ether | 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). CAS No. 50856-26-3. Product ID: ethane-1,2-diol; ethenol. Molecular formula: average Mn 250. Mole weight: C4H10O3. OC=C.OCCO. InChI=1S/C2H6O2.C2H4O/c3-1-2-4; 1-2-3/h3-4H, 1-2H2; 2-3H, 1H2. KMIMOJVUFBBNHO-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) linear dendrimer | Bis-MPA (or 2,2-Bis(methylol)propionic acid) is an aliphatic, pro-chiral molecule comprised of two hydroxyls and one carboxylic group that has been used in the synthesis of many different types of polymers. Uses: Dendrons synthesized from bis-mpa are biodegradable and have low cytotoxicity, making them well suited for use in biological research s. these materials have been used in many s such as signal amplification in bioassays and in drug delivery s. peg-core dendrimers feature excellent solubility in water and a high degree of functionality per peg chain, making them strong candidates for advanced drug delivery systems or as targeting vessels. additionally, the terminal amine groups can readily be used in edc or dcc coupling reactions (after boc deprotection) with carbonyl-containing compounds, to yield highly functionalized materials for a variety of biomedical s. Group: Dendrimers. Alternative Names: PFD-G2-PEG6k-NHBOC, Dendron bifunctionalized PEG. Molecular formula: 8075.40. | |
| Poly(ethylene glycol) linear dendron | Bis-MPA (or 2,2-Bis(methylol)propionic acid) is an aliphatic, pro-chiral molecule comprised of two hydroxyls and one carboxylic group that has been used in the synthesis of many different types of polymers. Uses: Dendrons synthesized from bis-mpa are biodegradable and have low cytotoxicity, making them well suited for use in biological research s. these materials have been used in many s such as signal amplification in bioassays and in drug delivery s. peg-core dendrons feature excellent solubility in water and a high degree of functionality per peg chain, making them strong candidates for advanced drug delivery systems or as targeting vessels. additionally, the terminal amine groups can readily be used in edc or dcc coupling reactions (after boc deprotection) with carbonyl-containing compounds, to yield highly functionalized materials for a variety of biomedical s. Group: Dendrimers. Alternative Names: PFD-G4-PEG2k-NHBOC, Dendron functionalized PEG. Molecular formula: 6495.23. CC (COC (CCNC (OC (C) (C) C) = O) = O) (C (OCC (C (OCC (C (OCC (C (OCC OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC OCCOCCOCCOCCOCCOCCOCCOCCOC) = O) (C ) COC (C (COC (C (COC (C (COC (CCNC (OC (C) (C) C) = O) = O) (C) COC ( CCNC (OC (C) (C. | |
| Poly(ethylene glycol) methacrylate | Poly(ethylene glycol) methacrylate. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 25736-86-1. | |
| Poly(ethylene glycol) methyl ether | Poly(ethylene glycol) methyl ether. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 9004-74-4. | |
| Poly(ethylene glycol) methyl ether (2-methyl-2-propionic acid dodecyl trithiocarbonate) | Poly(ethylene glycol) methyl ether (2-methyl-2-propionic acid dodecyl trithiocarbonate). Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol) methyl ether (4-cyano-4-pentanoate dodecyl trithiocarbonate) | Poly(ethylene glycol) methyl ether (4-cyano-4-pentanoate dodecyl trithiocarbonate). Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol)methyl ether acetylene | Poly(ethylene glycol)methyl ether acetylene. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Poly(ethylene glycol) methyl ether acrylate | 2-methoxyethyl acrylate is a clear colorless liquid with a sharp musty odor. (NTP, 1992);Liquid. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 32171-39-4. Product ID: 2-methoxyethyl prop-2-enoate. Molecular formula: 130.14g/mol. Mole weight: C6H10O3. COCCOC(=O)C=C. InChI=1S/C6H10O3/c1-3-6 (7)9-5-4-8-2/h3H, 1, 4-5H2, 2H3. HFCUBKYHMMPGBY-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) methyl ether amine | 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). Alternative Names: methoxyPEG amine, PEG NH2, mPEG-NH2, Methoxypolyethylene glycol amine, mPEG amine. CAS No. 80506-64-5. Pack Sizes: Packaging 1 mL in glass bottle. Product ID: 2- [2- [2- [2- [2- [2- [2- [2- [2- [2- [2- (2-methoxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethanamine. Molecular formula: PEG average Mn 450 (n~1 | |
| Poly(ethylene glycol) methyl ether azide | 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: Peg functionalized with azide is commonly used in copper-mediated ligation (click chemistry). peg of this molecular weight should remain amorphous at room temperature. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Methoxypolyethylene glycol azide, mPEG-N3, azido mPEG, PEG N3, methoxyPEG azide, mPEG azide. CAS No. 89485-61-0. Pack Sizes: Packaging 1 mL in glass bottle. Molecular formula: PEG average Mn 350 (n~8) average Mn 400. | |
| Poly(ethylene glycol) methyl ether-block-poly(D,L lactide) | Poly(ethylene glycol) methyl ether-block-poly(D,L lactide) is an amphiphilic, diblock copolymer composed of a hydrophilic PEG block and a hydrophobic PLA block. Uses: Due to these properties, these polymers are widely used in polymeric nanoparticle formulation to achieve controlled and targeted delivery of therapeutic agents (e.g. apis, genetic material, peptides, vaccines, and antibiotics). Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: mPEG-PLLA, Biodegradable, PLLA, PEG-PLA, Drug delivery, mPEG-PLA, Block copolymer. Pack Sizes: 1 g in glass bottle. Molecular formula: PDLA average Mn 20,000 (by NMR) PDLLA average Mn 20000 PEG average Mn 5,000 (by NMR) PEG average Mn 5000. Mole weight: HO[CH(CH3)COO]m[CH2CH2O]nCH3. | |
| Poly(ethylene glycol) methyl ether-block-poly(D,L lactide)-block-decane | Block copolymer micelles are widely used in drug delivery applications. PEG-PDLLA is a biodegradable polymeric micelle which is used as carriers for hydrophobic drugs like paclitaxel. PEG is the hydrophilic part and PDLLA is the hydrophobic part which forms the micelle core wherein the hydrophobic drug is loaded. Uses: Used as a carrier for the controlled and targeted release of anticancer hydrophobic drugs. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-PDLLA-decane, PEG-b-PLA-b-decane, PEG-PLA. Pack Sizes: 1 g in glass bottle. Molecular formula: PDLLA average Mn 2,000 PEG average Mn 2,000 average Mn 4,000 (total). | |
| Poly(ethylene glycol) methyl ether-block-poly(ε-caprolactone) | This polymer product is biodegradable. Uses: Biodegradable polymer for drug delivery. Group: Biodegradable polymers. Alternative Names: PEG-PCL, PEG-b-PCL. Pack Sizes: 1 g in glass bottle. Molecular formula: PCL average Mn 25,000 PEG average Mn 5,000 apparent mol wt 20000-30000 (PCL) apparent mol wt 4000-6000 (PEG). Mole weight: CH3(C2H4O)nO(C6H10O2)mH. | |
| Poly(ethylene glycol) methyl ether-block-poly(lactide-co-glycolide) | Contains ≤500 ppm impurities by GC, including trace monomer and residual organics. Uses: Biocompatible block copolymer. can be used in the formation of nanoparticles for drug delivery. potential use in the targeted and/or controlled release of cancer drugs, anti-inflammatory drugs, antibiotics, or anesthetic agents. Group: Biodegradable polymerspoly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-PLGA, mPEG-b-PLGA. Molecular formula: PEG average Mn 5,000 PLGA Mn 5,000. Mole weight: H[(C3H4O2)x(C2H2O2)y]mO[C2H4O]nCH3. | |
| Poly(ethylene glycol) methyl ether-block-poly(L-lactide-co-glycolide) | Poly(L-lactide-co-glycolide) (PLGA) is a biodegradable and biocompatible copolymer for use in biomedical research devices, such as grafts, sutures, implants. Uses: Amphiphilic block copolymers (ambc) are made up of two chemically different homopolymer blocks. one of the block is hydrophilic and the other one is hydrophobic. these macromolecules have the properties to self-assemble when dissolved in an aqueous media. peg-plga is one the most commonly used biodegradable amphiphilic block copolymers for drug delivery applications. peg is the hydrophilic part and plga is the hydrophobic part.used in the synthesis of targeted nanoparticles which are used for differential delivery and controlled release of drugs. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: PEG-PLGA, PEG-b-PLGA. Pack Sizes: 1 g in glass bottle. Molecular formula: PEG average Mn 5,000 PLGA average Mn 25,000. Mole weight: CH3[C2H4O]nO[(C2H2O2)x(C3H4O2)y]mH. | |
| Poly(ethylene glycol) methyl ether maleimide | 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: Poly(ethylene glycol) methyl ether maleimide is a maleimide-functionalized poly(ethylene glycol). due to the maleimide-functionalization, this material can be used to rapidly conjugate thiol-containing biomolecules, apis, or targeting ligands. Group: Poly(ethylene glycol) and poly(ethylene oxide). Alternative Names: Methoxy PEG maleimide, PEG methyl ether maleimide. Pack Sizes: Packaging 1, 5 g in glass bottle. Molecular formula: average Mn 2000. | |
| Poly(ethylene glycol) methyl ether methacrylate | Poly(ethylene glycol) methyl ether methacrylate. Group: Poly(ethylene glycol) and poly(ethylene oxide)polymers. CAS No. 26915-72-0. Product ID: 2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate. Molecular formula: 276.33g/mol. Mole weight: C13H24O6. CC(=C)C(=O)OCCOCCOCCOCCOC. InChI=1S / C13H24O6 / c1-12 (2) 13 (14) 19-11-10-18-9-8-17-7-6-16-5-4-15-3 / h1, 4-11H2, 2-3H3. KRCGBOKYIUDIFY-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) methyl ether methacrylate solution | Poly(ethylene glycol) methyl ether methacrylate solution. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 26915-72-0. Product ID: 2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate. Molecular formula: 276.33g/mol. Mole weight: C13H24O6. CC(=C)C(=O)OCCOCCOCCOCCOC. InChI=1S / C13H24O6 / c1-12 (2) 13 (14) 19-11-10-18-9-8-17-7-6-16-5-4-15-3 / h1, 4-11H2, 2-3H3. KRCGBOKYIUDIFY-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) methyl ether thiol | Poly(ethylene glycol) methyl ether thiol. Group: Poly(ethylene glycol) and poly(ethylene oxide). | |
| Polyethylene glycol monomethyl ether mesylate | Polyethylene glycol monomethyl ether mesylate. Group: Poly(ethylene glycol) and poly(ethylene oxide). CAS No. 175172-61-9. Product ID: 2-methoxyethyl methanesulfonate. Molecular formula: 154.19g/mol. Mole weight: C4H10O4S. COCCOS(=O)(=O)C. InChI=1S/C4H10O4S/c1-7-3-4-8-9(2, 5)6/h3-4H2, 1-2H3. BCKAHDGFNHDQST-UHFFFAOYSA-N. | |
| Poly(ethylene glycol) [N-(2-maleimidoethyl)carbamoyl]methyl ether 2-(biotinylamino)ethane | 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). Alternative Names: Biotin-PEG, Biotin polyoxyethylene maleimide, Biotin-PEG-maleimide, Biotinylated PEG. Pack Sizes: Packaging 100 mg in glass insert. Molecular formula: PEG average Mn 5000 (n~110) average Mn 5,400. | |
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