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| Product | Description | |
|---|---|---|
| Poly(hydroxyethyl methacrylate), DDMAT terminated | The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Poly(hydroxyethyl methacrylate) is a hydrophobic polymer which contains a hydrophilic hydroxy group. the end group functionality contains a carboxylic acid (cooh) as well as the 2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid raft agent moiety. this will allow for additional polymerization to generate a diblock copolymer. this raft agent is especially suited for the polymerization of styrene; acrylate and acrylamide monomers. Group: other plastics. Alternative Names: PolyHEA, PHEA, PolyHEMA, PHEMA, RAFT polymer, Macro RAFT-CTA. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 7,000. Mole weight: C4H7O2(C6H10O3)nC13H25S3. |  |
| Poly(N, N-dimethylacrylamide), DDMAT terminated | Poly(N, N-dimethylacrylamide), DDMAT terminated. Group: other plastics. | |
| Poly(N,N-dimethylacrylamide), DDMAT terminated | Need help choosing the correct RAFT Agent? Please consult the RAFT Agent to Monomer compatibility table. Uses: Poly(n; n-dimethylacrylamide) is generally used in biological s. additionally; the alpha-chain end is a functional carboxylic acid (for potential specialty/coupling reactions). ddmat is especially suited for the polymerization of styrene; acrylate; and acrylamide monomers to make lithographically and biologically important block copolymers. useful as a chain transfer agent (cta) or a functionalized polymer. Group: Hydrophilic polymers. Alternative Names: polydimethylacrylamide methylpropionic acid dodecyltrithiocarbonate, PDMAM, polyDMAM. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 10,000. Mole weight: HOCOCH (CH3)2 (CH2CHCON (CH3)2)nSCS2C12H25. | |
| Polystyrene-block-poly(acrylic acid), DDMAT terminated | Polystyrene-block-poly(acrylic acid), DDMAT terminated. Uses: Polystyrene-block-polyacrylic acid is a diblock copolymer commonly used for making polymeric vesicles (polymersomes) and other encapsulation applications.; this was generated through raft polymerization;and contains end-group functionalization that can be used to generate a triblock copolymer or modified for ligation. the 2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid raft agent cta is especially suited for the polymerization of styrene;acrylate and acrylamide monomers. Group: Polystyrene (ps). Mole weight: HOCOC (CH3)2 (CH2CHC6H5)m (CH2CHCOOH)nSCSSC12H25. | |
| Polystyrene, DDMAT terminated | Polystyrene is a colorless and transparent thermoplastic, among which expanded polystyrene is commonly known as Styrofoam. Uses: Poly(styrene) is a hydrophobic polymer used in many s. Group: Polystyrene (ps). Alternative Names: Poly(styrene) RAFT. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 10,000. Mole weight: C4H7O2(C8H8)nC13H25S3. | |
| Poly(tert-butyl acrylate), DDMAT terminated | Poly(tert-butyl acrylate), DDMAT terminated. Group: Hydrophilic polymers. | |
| Poly(tert-butyl acrylate), DDMAT terminated, azide terminated | Poly(tert-butyl acrylate) is a hydrophobic polymer used in many applications; primarily in which the tert-butyl group is substituted with a desired functionality. The hydrophilicity of this block can be tuned by varying the hydrolysis of the t-butyl group. The end group functionality contains an azide as well as the 2-(Dodecylthiocarbonothioylthio)-2-methylpropionic acid RAFT agent moiety. Uses: This raft cta will allow for additional polymerization to generate a diblock copolymer. this raft agent is especially suited for the polymerization of styrene; acrylate and acrylamide monomers. Group: Hydrophilic polymers. Alternative Names: poly(t-butyl acrylate) RAFT. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 8,500. | |
| Poly(ethylene glycol) methyl ether 2-(dodecylthiocarbonothioylthio)-2-methylpropionate | 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: Polyethylene (pe). Alternative Names: Methoxy poly(ethylene oxide)-2-(dodecylthiocarbonothioylthio)-2-methylpropionate, PEG DDMAT macroCTA. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 1,100. | |
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