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Heterocyclic Organic Compound. Alternative Names: ACRYLOXY TERMINATED POLYDIMETHYLSILOXANES;(3-ACRYLOXY-2-HYDROXYPROPYL) TERMINATED POLYDIMETHYLSILOXANE;Siloxanes and Silicones, di-Me, acrylate-terminated;POLYDIMETHYLSILOXANE, ACRYLOXY TERMINATED: VISCOSITY 60-140 CST.;POLYDIMETHYLSILOXANE, ACRYLOXY TER. CAS No. 128754-61-0. Density: 1 g/cm3. Catalog: ACM128754610.
4-arm Poly(ethylene glycol) norbornene 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 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-norbornene, PEG-nb. CAS No. 1191287-92-9. Mole weight: average Mn 10000. Catalog: ACM1191287929-1.
4-arm Poly(ethylene glycol) norbornene 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 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-norbornene, PEG-nb. CAS No. 1191287-92-9. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 10000.
Silicon Flame Retardant. Alternative Names: Silicone Oil. CAS No. 128446-57-1. Mole weight: 500-1000. Appearance: Straw to amber Liquid. Slightly viscous. Catalog: ACM128446571.
Oxygen-terminated monolayer Ti3C2
Oxygen-terminated monolayer Ti3C2. Uses: Nano-adsorption, biosensors, ion screening, catalysis, lithium-ion batteries, supercapacitors, lubrication and many other fields. Group: Mxenes materials. ≥98%.
Phenoxy-terminated carbonate oligomer of Tetrabromobisphenol A
It is a brominated, aromatic Flame Retardant for thermoplastic resin systems. It is a white powder, offers excellent thermal stability, good UV stability and color.unique combination of properties makes it a suitable flame retardant in PBT, PET, PBT/PET blends, PC, ABS, ABS/PC blends, Polysulfone and SAN. The UV stability allows it to be formulated for applications subjected to indoor fluorescent and casual outdoor sunlight exposure. In addition, the high purity makes it a solid choice for applications requiring excellent electrical and thermal properties. Uses: Mainly use for pbt, pet, pbt/pet blends, pc, abs, abs/pc blends, polysulfone and san. Group: Brominated flame retardant. CAS No. 71342-77-3. Molecular formula: (C7H2Br3O2). (C16H10Br4O3)n. (C6H2Br3O). Appearance: White Powder. Catalog: ACM71342773-1.
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 1% Pt
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 1% Pt. Uses: Neutral Intermediate reactivity, useful for slow room temperature cures and moderate (30-100°C) higher temperature cures. Group: Platinum Catalysts. CAS No. 68478-92-2. Product ID: PC076.
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 2% Pt
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 2% Pt. Uses: Neutral Intermediate reactivity, useful for slow room temperature cures and moderate (30-100°C) higher temperature cures. Group: Platinum Catalysts. CAS No. 68478-92-2. Product ID: PC075.
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 3% Pt
Platinum-Divinyltetramethyldisiloxane Complex in vinyl terminated polydimethylsiloxane - 3% Pt. Uses: Neutral Intermediate reactivity, useful for slow room temperature cures and moderate (30-100°C) higher temperature cures. Group: Platinum Catalysts. CAS No. 68478-92-2. Product ID: PC075.3.
Poly(2-ethyl-2-oxazoline), alkyne terminated
2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Polyoxazolines with alkyne end functional groups can be covalently attached to azide groups through copper-mediated ligation. polyoxazolines are biocompatible; hydrophilic; amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: Alkyne-PEtOx-OH. CAS No. 1171957-24-6. Molecular formula: C3H3(C5H9NO)nOH. Mole weight: average Mn 10,000. Catalog: ACM1171957246-1.
Poly(2-ethyl-2-oxazoline), alkyne terminated
2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Polyoxazolines with alkyne end functional groups can be covalently attached to azide groups through copper-mediated ligation. polyoxazolines are biocompatible; hydrophilic; amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: Alkyne-PEtOx-OH. CAS No. 1171957-24-6. Pack Sizes: Packaging 500 mg in glass bottle. Molecular formula: average Mn 10,000. Mole weight: C3H3(C5H9NO)nOH.
2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Poly(2-ethyl-2-oxazoline) is a hydrophilic polymer that is commonly used in biomedical s. this is a biocompatible polymer with one chain-end functionalized with a thiol group which is commonly used in ligation as well as in thiol-ene click chemistry. these polymers are commonly used as an amorphous alternative to pegs. Group: Hydrophilic polymers. Alternative Names: Polyoxazoline, PEtOx, POx. Pack Sizes: Packaging 5 g in glass bottle. Molecular formula: average Mn 10,000. Mole weight: C6H5CH2(C5H9NO)nSH.
2-Ethyl-2-oxazoline is an oxazoline which is used particularly as a monomer for the cationic ring-opening polymerization to poly(2-alkyloxazoline)s. This type of polymers are under investigation as readily water-soluble and biocompatible materials for biomedical applications. Uses: Amine polyoxazolines can be covalently attached through conjugation to carboxyl groups or sulfhydryl groups. amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination. polyoxazolines are a biocompatible, hydrophilic, amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: aminoPEOx, Poly(2-ethyl-2-oxazoline) hydroxyethyl amine, POZ, Polyoxazoline, amino terminated polyoxazoline. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 2,000. Mole weight: CH3(C5H9NO)nNHC2H4OH.
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Polyoxazolines with azide end functional group can be covalently attached to alkyne groups through copper-mediated ligation. polyoxazolines are a biocompatible, hydrophilic, amorphous alternatives to poly(ethylene glycol). Group: Hydrophilic polymers. Alternative Names: Azidopolyoxazoline, Azidopolymethyloxazoline 5kDa. Pack Sizes: Packaging 1 g in glass bottle. Molecular formula: average Mn 5,000. Mole weight: C6H5CH2(C5H9NO)nN3.
Poly(2-methyl-2-oxazoline), hydroxy terminated
The hydrophilic polymer contains polar or charged functional groups, making it soluble in water. Uses: Poly(2-methyl-2-oxazoline) is a hydrophilic polymer that is commonly used in biomedical s. this is a biocompatible polymer with one chain-end functionalized with an oh group. they are commonly used as an amorphous alternative to peg's. Group: Hydrophilic polymers. Alternative Names: PMOx, POx 5kDa. Pack Sizes: Packaging 5 g in glass bottle. Molecular formula: average Mn 5,000. Mole weight: CH3(C4H7NO)nOH. 1S/C5H11NO2/c1-5(8)6(2)3-4-7/h7H, 3-4H2, 1-2H3. OBSKGKGKPGOOTB-UHFFFAOYSA-N.
The polymer product is a hydrophobic material that is insoluble in water or other polar solvents. Uses: Component of epoxy-based adhesives, composites and coatings. intermediate in corrosion-resistant vinyl esters, acrylated epoxies used in radiation curing and photopolymer printing plates. Group: other plastics. CAS No. 68891-46-3. Pack Sizes: 250 mL in poly bottle. Product ID: buta-1,3-diene; prop-2-enenitrile. Molecular formula: average Mn ~3,800. Mole weight: HO2C[CH2CH(CN)]x(CH2CH=CHCH2)yCO2H. C=CC=C.C=CC#N. InChI=1S/C4H6.C3H3N/c1-3-4-2; 1-2-3-4/h3-4H, 1-2H2; 2H, 1H2. NTXGQCSETZTARF-UHFFFAOYSA-N.
Polybutadiene, dicarboxy terminated
Polybutadiene, dicarboxy terminated. Group: Hydrophobic polymers. Alternative Names: CTPB. CAS No. 68891-79-2.
Polybutadiene, phenyl terminated
Polybutadiene is a synthetic rubber. Polybutadiene rubber is a polymer formed from the polymerization of the monomer 1,3-butadiene. Uses: Polybutadiene has a high resistance to wear. Group: Hydrophobic polymers. Pack Sizes: 100 g in glass bottle. Molecular formula: average Mn ~1,800. C=CC=C.
Tandem mass spectrometry (MS/MS) reveals that bis(3-aminopropyl)-PDMS mainly dissociates via intramolecular nucleophilic substitutions at the end groups. Uses: Bis(3-aminopropyl) terminated poly(dimethylsiloxane) may be used in the synthesis of dipicolylamidopropylpoly (dimethylsiloxane) (dppdms). Group: 3d printing materials bioelectronic materials self assembly and lithography. Alternative Names: PDMS. CAS No. 106214-84-0. Pack Sizes: 50 mL in poly bottle. Product ID: 3-[[[3-aminopropyl(dimethyl)silyl]oxy-dimethylsilyl]oxy-dimethylsilyl]propan-1-amine. Molecular formula: average Mn ~2500. Mole weight: H2N (CH2)3Si (CH3)2O[Si (CH3)2O]nSi (CH3)2 (CH2)3NH2. C[Si](C)=O.C[Si](C)(O)CCCN. InChI=1S/C12H34N2O2Si3/c1-17(2, 11-7-9-13)15-19(5, 6)16-18(3, 4)12-8-10-14/h7-14H2, 1-6H3. ZWRBLCDTKAWRHT-UHFFFAOYSA-N.
Micro/NanoElectronics. Alternative Names: POLY(DIMETHYLSILOXANE), DIGLYCIDYL ETHER TERMINATED;Poly(diMethylsiloxane), diglycidyl ether terMinated Mn ~800. CAS No. 130167-23-6. Purity: 0.96. Catalog: ACM130167236.
Poly(Dimethylsiloxane), Distearate Terminated
Siloxane Compound. CAS No. 130169-63-0. Molecular formula: C26H52O2S2. Catalog: ACM130169630-1.
Poly(dimethylsiloxane), hydride terminated
Poly(dimethylsiloxane), hydride terminated. Group: Bioelectronic materials self assembly and lithography. Alternative Names: Hydrogen-terminated di-Me silicones. CAS No. 70900-21-9. Pack Sizes: 100 mL in poly bottle. Product ID: bis(dimethylsilyloxy)-dimethylsilane. Molecular formula: 208.48g/mol. Mole weight: C6H20O2Si3. C[Si](C)=O. InChI=1S/C6H20O2Si3/c1-9(2)7-11(5, 6)8-10(3)4/h9-10H, 1-6H3. HZBDPZBVINJJET-UHFFFAOYSA-N.
Poly(dimethylsiloxane), hydroxy terminated
Poly(dimethylsiloxane), hydroxy terminated. Uses: Component of silicone room temperature vulcanizing system that incorporates reinforcing aids or fillers. Group: Bioelectronic materials self assembly and lithography. Alternative Names: PDMS. CAS No. 70131-67-8. Pack Sizes: 250 mL in poly bottle. C[Si](C)(O)O.
We provide you with RAFT agent for radical controlled polymerization. Uses: Reversible addition fragmentation chain transfer (raft) polymerization. Group: 3d printing materials biodegradable polymers. Alternative Names: RAFT-PLA, PDLLA RAFT terminated. Pack Sizes: 1 g in glass bottle. Molecular formula: average Mn 10,000.
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.
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 oxide), 4-arm, amine 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 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). Molecular formula: average Mn 10000.
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). Molecular formula: average Mn 10000.
Poly(ethylene oxide), 4-arm, hydroxy 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 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). Molecular formula: average Mn 10000.
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). Molecular formula: average Mn 10000.
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