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functionalization

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Castor oil
Xenaderm, Venelex, Ricinus Oil
T32538001-79-4
Castor oil (Xenaderm) is a vegetable oil pressed from the seeds of the castor bean, Ricinus communis, used as a laxative and as an excipient in medicinally.
  • $29
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Fmoc-His(Trt)-OH
T67561109425-51-6
Fmoc-His(Trt)-OH is a synthetically derived organic compound utilized in life science research. (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanoic acid provides a reactive platform for peptide synthesis, functionalization, and chemical biology studies.
  • $29
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DSPE-PEG-NHS(MW 3400)
DSPE-PEG-NHS, MW 3400, DSPE-PEG-NHS(MW 3400)
T772851244784-44-8
DSPE-PEG-NHS(MW 3400)is a PEGylated phospholipid derivative designed for advanced lipid formulation applications, particularly in the preparation of liposomes, where it enables efficient surface modification and functionalization, and is widely used as a delivery material for nucleic acid-based therapeutics such as DNA and mRNA vaccines, supporting research in drug delivery systems, nanomedicine, and vaccine formulation technologies.
  • $29
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(+)-JQ1 maleimide
T83929
(+)-JQ1 maleimide, featuring a cysteine-reactive maleimide linked to the BRD4 ligand, JQ1, via a PEG2 linker, serves as a probe suitable for the COFFEE method (COvalent Functionalization Followed by E3 Electroporation). This approach facilitates the covalent attachment of (+)-JQ1 maleimide to VHL, followed by electroporation into live cells, where the E3 ligase complexes with intracellular BRD4 to prompt its degradation.
  • $1,180
35 days
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H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride
T878352560614-20-0
H-L-Lys(Norbornene-methoxycarbonyl)-OH hydrochloride is a norbornene-derivatized lysine capable of undergoing click-functionalization. This compound facilitates the mild and selective modification of proteins through a copper-free click reaction [1].
  • $1,520
4-6 weeks
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QTY
mPEG-CHO (MW 350)
mPEG-CHO (MW 350), mPEG-Aldehyde (MW 350)
TCL-00473
mPEG-CHO (MW 350) participates in the formation of three-dimensional porous scaffolds and acts as a delivery vehicle by carrying active substances. The -CHO functional group interacts with the -NH2 functional group of the chitosan chain to form a glutaraldehyde-type adduct, functionalizing mPEG. This functionalization and cross-linking can affect the rigidity of the delivery system, enabling the cross-linked conjugated system to have a slow-release function.
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mPEG-CHO (MW 550)
mPEG-CHO (MW 550), mPEG-Aldehyde (MW 550)
TCL-00474
mPEG-CHO (MW 550) is involved in the formation of three-dimensional porous scaffolds and acts as a delivery carrier for active substances. The -CHO functional group interacts with the -NH2 functional group of chitosan chains to form a glutaraldehyde-type adduct, functionalizing the mPEG. This functionalization and cross-linking can affect the rigidity of the delivery system, enabling the cross-linked conjugate system to possess slow-release capabilities.
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mPEG-CHO (MW 750)
mPEG-CHO (MW 750), mPEG-Aldehyde (MW 750)
TCL-00475
mPEG-CHO (MW 750) is involved in the formation of three-dimensional porous scaffolds and acts as a delivery vector when carrying active substances. The -CHO functional group interacts with the -NH2 functional group of chitosan chains to form a glutaraldehyde-like adduct, resulting in the functionalization of mPEG. This functionalization and crosslinking can affect the rigidity of the delivery system, enabling the crosslinked conjugated system to have a slow release function.
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mPEG-CHO (MW 1000)
mPEG-CHO (MW 1000), mPEG-Aldehyde (MW 1000)
TCL-00476
mPEG-CHO (MW 1000) is involved in the creation of three-dimensional porous scaffolds and acts as a carrier for active substances. The -CHO functional group interacts with the -NH2 functional group on chitosan chains to form a glutaraldehyde-like adduct, thereby functionalizing mPEG. This functionalization and cross-linking influence the rigidity of the delivery system, enabling the cross-linked conjugated system to possess slow-release capabilities.
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mPEG-CHO (MW 2000)
mPEG-CHO (MW 2000), mPEG-Aldehyde (MW 2000)
TCL-0047770086-22-9
mPEG-CHO (MW 2000) is involved in the formation of three-dimensional porous scaffolds and acts as a delivery carrier when combined with active substances. The -CHO functional group interacts with the -NH2 functional group of chitosan chains to form a glutaraldehyde-type adduct, thereby functionalizing mPEG. This process of functionalization and crosslinking can affect the rigidity of the delivery system, enabling the crosslinked conjugate system to possess a slow-release function.
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mPEG-CHO (MW 3400)
mPEG-CHO (MW 3400), mPEG-Aldehyde (MW 3400)
TCL-00478
mPEG-CHO (MW 3400) participates in the formation of three-dimensional porous scaffolds and acts as a delivery carrier when combined with active substances. The -CHO functional group interacts with the -NH2 functional group of the chitosan chain to form a glutaraldehyde-type adduct, thus functionalizing mPEG. This functionalization and cross-linking can influence the rigidity of the delivery system, enabling the cross-linked conjugate system to have a slow release function.
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mPEG-CHO (MW 5000)
mPEG-CHO (MW 5000), mPEG-Aldehyde (MW 5000)
TCL-00479
mPEG-CHO (MW 5000) is involved in the formation of three-dimensional porous scaffolds and acts as a delivery carrier when combined with active substances. The -CHO functional group interacts with the -NH2 group of chitosan chains, forming a glutaraldehyde-type adduct that functionalizes mPEG. This process of functionalization and crosslinking affects the rigidity of the delivery system, enabling the crosslinked conjugate system to possess slow release capabilities.
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mPEG-CHO (MW 10000)
mPEG-CHO (MW 10000), mPEG-Aldehyde (MW 10000)
TCL-00480
mPEG-CHO (MW 10000) contributes to the formation of three-dimensional porous scaffolds and serves as a delivery vehicle when carrying active substances. The -CHO functional group interacts with the -NH2 group of chitosan chains to form a glutaraldehyde-type adduct, thereby functionalizing mPEG. This functionalization and cross-linking affect the rigidity of the delivery system, enabling the cross-linked conjugate system to have a slow release function.
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mPEG-CHO (MW 20000)
mPEG-CHO (MW 20000), mPEG-Aldehyde (MW 20000)
TCL-00481
mPEG-CHO (MW 20000) plays a role in creating three-dimensional porous scaffolds and acts as a delivery vector by carrying active substances. The -CHO functional group interacts with the -NH2 functional group of chitosan chains, forming a glutaraldehyde-type adduct, thereby functionalizing mPEG. This functionalization and crosslinking can affect the rigidity of the delivery system, enabling the crosslinked conjugate system to possess a slow-release function.
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Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 1000)
165729-81-7
TCL-00823
Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 1000) is a derivative of polyethylene glycol. It is applicable in bioconjugation, drug delivery, PEG hydrogels, as a cross-linking agent, and for surface functionalization.
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Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 2000)
165729-81-7
TCL-00824
Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 2000) is a derivative of polyethylene glycol, which is utilized in applications such as bioconjugation, drug delivery, PEG hydrogels, crosslinking agents, and surface functionalization.
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Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 3400)
165729-81-7
TCL-00825
Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 3400) is a derivative of polyethylene glycol, suitable for use in bioconjugation, drug delivery, PEG hydrogels, cross-linkers, and surface functionalization.
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Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 5000)
165729-81-7
TCL-00826
Poly(ethylene glycol) 2-mercaptoethyl ether acetic acid (Mn 5000) is a derivative of polyethylene glycol, applicable in bioconjugation, drug delivery, PEG hydrogels, crosslinking agents, and surface functionalization.
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1-Pyrenamin
1-Pyrenamine (purified by sublimation), 1-Pyrenamin
TYD-007361606-67-3
1-Pyrenamine is a polycyclic aromatic hydrocarbon (PAH) derivative commonly used as a catalyst carrier in methanol batteries, with widespread application in research and experiments in the life sciences.
  • $29
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