1 3 dimethylaminopropyl 3 ethylcarbodiimide hydrochloride edc
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) is a water-soluble carbodiimide used as a coupling agent in organic synthesis and biochemical reactions. It facilitates the formation of amide bonds between carboxyl groups and primary amines.
Lab products found in correlation
12 protocols using 1 3 dimethylaminopropyl 3 ethylcarbodiimide hydrochloride edc
Multifunctional Nanoparticle Biosensing
Daunorubicin and Doxorubicin Nanoparticles
Synthesis of Multifunctional PEG-Based Hydrogels
and 4-arm PEG-amino succinic acid (PEG-ASA) (10 kDa) were purchased
from JenKem Technology and Laysan Bio Inc., respectively. Carbic anhydride,
pyridine, dichloromethane (DCM), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
hydrochloride (EDC) were all purchased from Thermo Scientific. 5-Norbornene-2-carboxylic
acid, tetrahydrofuran (THF), 4-dimethylaminopyridine (DMAP), and N,N′-dicyclohexylcarbodiimide (DCC)
were obtained from Sigma-Aldrich. Tetrazine-amine and methylTetrazine-amine
were purchased from Click Chemistry Tools. N-hydroxylsuccinimide
(NHS) and N,N-diisopropylethylamine
(DIEA) were obtained from Tokyo Chemical Industry (TCI). N,N-dimethylformamide (DMF), 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxide
hexafluorophosphate (HATU), and cold soluble gelatin were purchased
from Alfa Aesar, AnaSpec, and Modernist Pantry, respectively. Calcein-AM
and ethidium homodimer stains were obtained from Biotium. F-actin
stain was purchased from Cytoskeleton, Inc.
Synthesis and Characterization of PEG-PGlu Copolymers
Synthesis and Characterization of PLGA Nanoparticles
Synthesis of Bioactive PEG Hydrogel Precursors
Synthesis of High Molecular Weight γ-PGA Hydrogel
Graphene Oxide-Based Drug Delivery System
Retinol-Based Nanoparticle Synthesis
Stearic Acid Activation and Conjugation
acid groups of stearic acid was needed. It was achieved as described
in our previous study.39 (link) We dissolved 284
mg of stearic acid (MW: 284.48, Acros Organics, Geel, Belgium), 206
mg of 1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide hydrochloride
(EDC; Acros Organics, Geel, Belgium), 140 mg of N-hydroxysuccinimide (NHS; Acros Organics, Geel, Belgium), and 0.250
mL of triethanol amine (TEA; Molekula GmbH, Munich, Germany) in 20
mL of DMSO in a beaker. We stirred the mixture for 2 h at 80 °C
and another 24 h at RT. In addition, we slowly added the activated
solution containing stearic acid to the CSFI solution, stirred for
10 h at 60 °C, and kept it at RT for another 24 h. The resulting
solution (CSFISA) was stored at −20 °C until further use.
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