N boc ethanolamine

Manufactured by Merck Group

Sourced in China

N-Boc-ethanolamine is a chemical compound used as a building block in organic synthesis. It is a protected amino alcohol with a tert-butyloxycarbonyl (Boc) protecting group. The compound is commonly used as a versatile intermediate in the preparation of various pharmaceutical and other chemical products.

Automatically generated - may contain errors

Lab products found in correlation

3 protocols using n boc ethanolamine

Hyaluronic Acid-based Nanoparticles for Doxorubicin Delivery

Check if the same lab product or an alternative is used in the 5 most similar protocols

Hyaluronic acid, propylene sulfide, adipic
dihydrazide, caprolactone, N-Boc-ethanolamine, doxorubicin
hydrochloride (DOX·HCl), dicyclohexylcarbodiimide (DCC), 4-dimethylaminopyridine
(DMAP), ethyl-3-(3-dimethylaminopropyl) carbodiimidehydrochloride
(EDC·HCl), and N-hydroxysuccinimide (NHS) were
purchased from Sigma-Aldrich Co., Ltd. (Beijing, China). N,N-Dimethylformamide (DMF) and triethylamine (TEA)
were purchased from Alfa Aesar Co., Ltd. (Shanghai, China). 2,7-Dichlorofluorescin
diacetate (DCFH-DA) was purchased from Yeasen Biotechnology Co., Ltd.
(Shanghai, China). 4′,6-Diamidino-2-phenylindole (DAPI), propidium
iodide (PI), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium
bromide (MTT), and TUNEL agents were obtained from Solarbio Co., Ltd.
(Beijing, China). Cell culture agents were purchased from GIBCO. Antibodies
were acquired from Abcam Co., Ltd. (Shanghai, China).

Yu Y., Feng Z., Liu J., Hou X., Zhou X., Gao J., Wang W., Zhang Y., Li G, & Liu J. (2021). γ-Ray-Triggered Drug Release of Reactive Oxygen Species-Sensitive Nanomedicine for Enhanced Concurrent Chemoradiation Therapy. ACS Omega, 6(30), 19445-19457.

+ Open protocol

+ Expand

Synthesis and Characterization of Oxonorbornene Monomers

Check if the same lab product or an alternative is used in the 5 most similar protocols

Reagent-grade maleic acid anhydride, furan, 1-butanol, 4-(dimethylamino)pyridine, dicyclohexyl carbodiimide, and N-Boc-ethanolamine, which were used for oxonorbornene monomer synthesis, were purchased from Sigma-Aldrich and used as received. Solvents needed for the synthesis including toluene (dry), tetrahydrofurane (dry), dichloromethane (freshly distilled from CaH₂), and n-hexane were purchased from Carl Roth. A Grubbs second-generation catalyst was purchased from Sigma-Aldrich; it was reacted with pyridine to form a Grubbs third-generation catalyst using a previously reported procedure.^{26 (link) 1}H NMR spectra were recorded on a Bruker 250 MHz spectrometer (Bruker, Madison, WI) to confirm the molecular structure of the oxonorbornene monomers and polymers. The molecular mass and mass distribution of the polymers were studied by gel permeation chromatography (GPC) using an Agilent GPC system with chloroform as eluent, PSS SDV columns (PSS, Mainz, Germany), and poly(methyl methacrylate) standards.

Zheng Z., Saar J., Zhi B., Qiu T.A., Gallagher M.J., Fairbrother D.H., Haynes C.L., Lienkamp K, & Rosenzweig Z. (2018). Structure–Property Relationships of Amine-rich and Membrane-Disruptive Poly(oxonorbornene)-Coated Gold Nanoparticles. Langmuir : the ACS journal of surfaces and colloids, 34(15), 4614-4625.

+ Open protocol

+ Expand

Synthesis of Radical Polymerization Reagents

Check if the same lab product or an alternative is used in the 5 most similar protocols

Phosphate-buffered
saline (PBS) solutions were
prepared using preformulated tablets (Sigma-Aldrich) in 200 mL of
Milli-Q water (>18.2 Ω mean resistivity) to give [NaCl] =
0.138
M, [KCl] = 0.0027 M, and pH 7.4. Vinyl acetate (>99%), styrene
(>99%),
and isopropenyl acetate (99%) were purchased from Sigma-Aldrich and
were filtered through a plug of basic alumina to remove inhibitors
prior to use. 4,4′-Azobis(4-cynaovaleric acid) (>98%) was
recrystallized
from methanol and stored at −18 °C in the dark. Maleic
anhydride (99%), benzyl bromide (98%), 2-cyano-2-propyl benzodithioate
(>97%), N-Boc-ethanolamine (98%), 2-dimethylaminoethanol (99.5%),
2-(diethylamino)ethanol (>99.5%), 2-(diisopropylamino)ethanol (>99%),
and trifluoroacetic acid (99%) were purchased from Sigma-Aldrich.
Potassium ethyl xanthate (98%) was purchased from Alfa Aesar. All
solvents were purchased from VWR or Sigma-Aldrich and used without
further purification. S-benzyl O-ethyl carbondithioate was synthesized by Thomas Congdon.^{41 (link)}

Stubbs C., Lipecki J, & Gibson M.I. (2016). Regioregular Alternating Polyampholytes Have Enhanced Biomimetic Ice Recrystallization Activity Compared to Random Copolymers and the Role of Side Chain versus Main Chain Hydrophobicity. Biomacromolecules, 18(1), 295-302.

+ Open protocol

+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Revolutionizing how scientists
search and build protocols!