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Dimethylformamide dmf

Manufactured by Merck Group
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Dimethylformamide (DMF) is a colorless, volatile, and flammable liquid compound commonly used as a solvent in various industrial and laboratory applications. It has the chemical formula C₃H₇NO. DMF is known for its high solubility and its ability to dissolve a wide range of organic and inorganic substances.

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231 protocols using dimethylformamide dmf

1

Polymeric Membrane Fabrication for Biomedical Applications

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Sodium hydroxide with a purity of 97% (NaOH), acetone, ethanol (99.5), hydrochloric acid, purity of 35–37% and glutaraldehyde (GA) (50%) was purchased from Wako Chemical Industries, Ltd Japan. Gentamicin sulfate salt (GENs), diclofenac sodium salt, polyacrylonitrile (PAN) with (average Mw 150,000), polyvinyl alcohol (PVA), (Mw: 85,000–124,000, 87–89% hydrolyzed), Dimethylformamide (DMF) were purchased from Aldrich Chemical.
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2

Synthesis and Characterization of Stimuli-Responsive Polymers

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Methacrylic acid (Merck, >99%) was distilled under vacuum before use. Azobis-isobutyronitrile (AIBN) is an initiator, which, was recrystallized from methanol former to use. Tetrahydrofuran (THF) (Scharlau, >99%), n-hexane (Merck, >99%), dimethylformamide (DMF) (Aldrich, 99%), dichloromethane (DCM) (Chem-Lab, >99.8%), chloroform (Mojallali, >99%), ethanol (Merck, 99.9%), methanol (Merck, 99.9%) were used as-purchased without further purification. N-isopropyl-acrylamide (NIPAM) (Aldrich) was recrystallized from n-hexane. Polyethylene glycol (PEG), biological grade, with molecular weight (Mw) of 4000 was supplied by the Sigma-Aldrich and used as received. 4,4′-azobis(4-cyanopentanoic acid) (75% Aldrich), bromobenzene (Aldrich, 99%), carbon disulfide (CS2, 99.9%), ethyl acetate, iodine (Aldrich, 99%) and magnesium sulphate (Aldrich, 98%), dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP), were used as-purchased without further purification.
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3

Synthesis and Characterization of Boc-PLL Polypeptide

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Boc-PLL polypeptide was synthesized by ring opening polymerization of the ε-tert-butyloxycarbonyl-L-lysine-N-carboxy anhydride (NCA), with the following molecular weight characteristics: Mw= 11,980 Daltons, Mn = 11,365 Daltons (degree of polymerization 50) and molecular polydispersity, Mw/Mn, = 1.054. Details are reported elsewhere [32 (link)]. PAA (Mw = 450,000 Daltons) was purchased from Polysciences (Warrington, USA). N, N′-Dicyclohexylcarbodiimide (DCC, Alfa Aesar, MA, USA), 1-Hydroxybenzotriazole hydrate (HOBt, Fluka, NC, USA) were used as received. Dimethylformamide (DMF, Aldrich, MA, USA), hydrochloric acid (HCl, Panreac, Chicago, IL, USA), sodium hydroxide (NaOH, Panreac, Chicago, IL, USA), diethyl ether (DEE), tetrahydrofuran (THF), methanol and trifluoroacetic acid (TFA) were purchased from Sigma-Aldrich (Athens, Greece) and used without further purification. Deuterated solvents deuterium oxide (D2O and deuterated dimethyl sulfoxide (DMSO-d6)) (from Sigma-Aldrich, St. Louis, MO, USA) were used as received. Ultra-pure 3-distilled water (3D-H2O) was obtained by means of an ELGA Medica R7/15 device.
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4

Synthesis and Characterization of NIPAM-NtBAM Copolymers

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The monomers N-isopropylacrylamide (NIPAM) and N-tert-butylacrylamide (NtBAM) were used as acquired by Fluorochem (Derbyshire, UK) and Alfa Aesar (Ward Hill, MA, USA), respectively. Potassium peroxodisulfate (KPS, Fluorochem, Derbyshire, UK), 2-aminoethanethiol hydrochloride (ET HCl, Alfa Aesar, Ward Hill, MA, USA), N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC, Alfa Aesar, Ward Hill, MA, USA) and 1-Hydroxybenzotriazole hydrate (HOBt, Fluka, NC, USA) were used as received. Dimethylformamide (DMF, Aldrich, St. Louis, MO, USA), hydrochloric acid (HCl, Panreac, IL, USA), sodium hydroxide (NaOH, Panreac, IL, USA), deuterated water (D2O, Sigma-Aldrich, St. Louis, MO, USA) and Dulbecco’s modified Eagle’s medium (DMEM, Sigma-Aldrich, St. Louis, MO, USA) were used as obtained by the provider without purification. Ultrapure water was received by an ELGA Medica-R7/15 device (ELGA Labwater, IL, USA).
Sodium alginate (NaALG, Sigma-Aldrich, St. Louis, MO, USA, no. 180947, molecular weight range: 120,000–190,000 g/mol, the ratio of mannuronic and guluronic units (M/G): 1.53) was further purified (a solution of 7% w/v NaALG in NaOH (0.005 M) was repeatedly purified by dialysis against ultrapure water (membrane MWCO: 12,000–14,000 Da), and the final NaALG product was obtained in its solid-state through lyophilization.
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5

Synthesis and Characterization of SIL M

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1-(3-aminopropyl)silatrane, SIL M, was prepared according to a procedure described in reference [11 (link)]. 2-hydroxy-5-nitrobenzaldehyde (Merck-Schuchardt) >98%, Acetonitrile (ACN) (Aldrich), chloroform (CHCl3) (Aldrich), dichloromethane (DCM) (Aldrich), dimethylformamide (DMF) (Aldrich), methanol (Aldrich), tetrahydrofuran (THF) (Aldrich) and dimethylsulfoxide (DMSO), Bovine Serum Albumin (BSA) (Sigma-Aldrich, Germany), Human Serum Albumin (HSA, 66.5 kDa, lyophilized powder, 96%) (Alpha-Aesar) were used as received.
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6

Flat-sheet Nanofibrous Adsorbents for Heavy Metal Removal

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PLA(LX175®) purchased from Filabot Co., Ltd. (Barre, VT, USA) and PEG-PPG-PEG (Pluronic® F-108) purchased from Sigma Aldrich, (St. Louis, MO, USA) were used as a polymer, which is a major component of the flat-sheet nanofibrous adsorbents; additionally, SiO2 purchased from Sigma Aldrich, which is a nanomaterial to be incorporated, was used. To prepare a solution for electrospinning, the following materials, as a solvent, were used: dichloromethane (DCM) and dimethylformamide (DMF) purchased from Sigma Aldrich without purification. To check the adsorption of heavy metal’s remove ability, used copper sulfate and hydrochloric acid (HCl) were purchased from Sigma Aldrich. Additionally, all water used in this study was deionized water.
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7

Quantifying Aflatoxins in Food Samples

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STG, aflatoxins (B1, B2, G1, G2 and M1), acetonitrile (ACN), methanol (MeOH), acetone, chloroform, n-heptane, sulphuric acid, disodium hydrogen phosphate, sodium dihydrogen phosphate, potassium dihydrogen phosphate, sodium carbonate, sodium bicarbonate, sodium chloride, magnesium sulphate, Tween 20, bovine serum albumin (BSA), keyhole limpet hemocyanin (KLH), horseradish peroxidase (HRP), sodium borohydride and dimethylformamide (DMF) were purchased from Sigma-Aldrich (Dorset, UK & Zwijndrecht, the Netherlands). Primary-secondary amine (PSA) bulk sorbent was purchased from Agilent (Amstelveen, the Netherlands). Substrate 3,3',5,5'-tetramethylbenzidine (TMB) for HRP enzyme was obtained from Neogen (Lansing, USA).
Samples were blended using IKA A11 Basic laboratory mill (IKA, Staufen, Germany) and centrifuged in Sigma 4K10 centrifuge (Sigma, Osterode am Harz, Germany). Microtiter plates were read on BioTek EL808 type ELISA plate reader (BioTek, Bad Friedrichshall, Germany).
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8

Extraction and Characterization of Moringa Components

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Fresh leaves, stems, seeds and roots of M. oleifera were collected from the Moringa Planting Base, located at the Chengmai Jinma Avenue, Haikou, Hainan, China on 24 February 2018. All the materials were freeze-dried once collected from the tree. All the samples were blended (Blender Philips HR2095/3) into powder separately and stored in −20 °C. A voucher specimen (voucher No: lm2013042304) was deposited in the Institute of Tropical Bioscience and Biotechnology, Academy of Science in Haikou, China.
Methanol, ethyl acetate (EA), trifluoroacetic acid (TFA), acetic acid, dimethylformamide (DMF), sodium sulfide (Na2S·9H2O), sodium chloride (NaCl), sodium sulfate (Na2SO4), allyl isothiocyanate (AITC, purity > 98%) and myrosinase (β-thioglucosidase, T4528-25 UN) were purchased from Sigma-Aldrich, Singapore. Phosphate buffered saline (PBS) was purchased from Vivantis Technologies Sdn. Bhd. (Selangor Darul Ehsan, Malaysia).
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9

Silver Nanoparticle Synthesis and Animal Study

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PCL (molecular weight [MW] =70,000), dimethylformamide (DMF) and dichloromethane were purchased from Sigma-Aldrich Co. (St Louis, MO, USA). DA hydrochloride was purchased from Solarbio Science & Technology Co., Ltd. (Beijing, People’s Republic of China). Silver nitrate (AgNO3) was purchased from Sangon (Shanghai, People’s Republic of China).
Animals were purchased from the Experimental Animal Department of the Third Military Medical University. All the experimental protocols were approved by the Institutional Animal Care and Use Committee of the Third Military Medical University, and all methods were performed according to the guidelines of the Third Military Medical University.
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10

Polymer-Based Solid Electrolyte Synthesis

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Poly(ethylene oxide-b-6-(4′-cyanobiphenyl-4-yloxy)hexylmethacrylate), PEO(5.0 kg/mol)-b-PMA/CB (4.5 kg/mol) (PDI = 1.15) was supplied by Polymer Source (Montreal, QC, Canada). The material was purified from ionic impurities by triple extraction in a dichloromethane/water mixture, and then thoroughly vacuum dried at 100 °C. Final drying and all subsequent preparation steps including the assembly of conductivity, SAXS and DSC cells were performed inside a glovebox (<4 ppm O2, <1 ppm H2O). Lithium perchlorate (LiClO4) (battery grade, 99.99%) and dimethyl formamide (DMF) (anhydrous, 99.8%) were used, as received from Sigma-Aldrich (St. Louis, MO, USA).
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