Phthalic anhydride
Phthalic anhydride is a chemical compound used as a raw material in the production of various industrial and consumer products. It is a colorless, crystalline solid with a characteristic odor. Phthalic anhydride is commonly used as an intermediate in the synthesis of phthalate plasticizers, alkyd resins, and other chemical derivatives.
Lab products found in correlation
33 protocols using phthalic anhydride
Graphene-based E. coli Sensor Development
Polyimide R-BAPB Synthesis and Reinforcement
The following fillers were used:
VGCF—carbon nanofibers obtained by gas phase deposition (Pyrograf®-III, Cedarville, OH, USA) with an outer diameter of ~100 nm and a length of 20 to 200 µm.
CF—discrete carbon fibers (Umatex, Moscow, Russia) with a diameter of ~7 µm and a length of ~7 mm.
Synthesis of Alkoxylated Polymer Resin
Example 5
13.6 g of a PEG-PPG-PEG block copolymer with —OH group functionality at each terminal end and having 1100 Daltons Mw (0.0124 moles) that is obtained from Sigma-Aldrich, 33.2 g of neopentyl glycol (0.31 moles, Sigma-Aldrich), and 48.7 g of phthalic anhydride (0.33 moles, Sigma-Aldrich) were weighed into a 250 ml 4-necked round bottom flask equipped with a heating mantle, overhead stirrer, temperature sensor, gas inlet, and a Dean-Stark trap with a condenser. The reaction was heated to 100° C. under a nitrogen atmosphere and 0.4 g p-toluene sulfonic acid monohydrate (0.002 moles, Sigma-Aldrich) as catalyst was added. The reaction was heated to 170-180° C. for 6 hours. The alkoxylated polymer resin that was produced was soft and had Mw of 2850 Daltons.
Lignin-based Biodegradable Polymer Composites
Purification and Characterization of Proteins
Synthesis of PEG-PPG-PEG Block Copolymer Resin
Example 4
13.6 g of a PEG-PPG-PEG block copolymer with —OH group functionality at each terminal end and having 1100 Daltons Mw (0.0124 moles) that is obtained from Sigma-Aldrich, 33.2 g of neopentyl glycol (0.31 moles, Sigma-Aldrich), and 46.2 g of phthalic anhydride (0.31 moles, Sigma-Aldrich) were weighed into a 250 ml 4-necked round bottom flask equipped with a heating mantle, overhead stirrer, temperature sensor, gas inlet, and a Dean-Stark trap with a condenser. The reaction was heated to 100° C. under a nitrogen atmosphere and 0.4 g p-toluene sulfonic acid monohydrate (0.002 moles, Sigma-Aldrich) as catalyst was added. The reaction was heated to 170-180° C. for 6 hours. The alkoxylated polymer resin that was produced was soft and tacky and had Mw of 1710 Daltons.
Synthesis and Characterization of PEG-Modified Biomaterials
following analytical-grade
chemicals were purchased from commercial sources and used without
further purification: glutamic acid, acetic anhydride, phthalic anhydride,
TTEGDA, PPS, PVP (Mw 40k and Mw 360k), sodium hydroxide (1 N), hydrochloric acid (1
N), anhydrous dichloromethane, anhydrous tetrahydrofuran (THF), anhydrous
methanol, anhydrous dimethyl sulfoxide (DMSO), O-[(N-succinimidyl)succinyl-aminoethyl-O′-methylpolyethylene
glycol (PEG-NHS, Mw 750), methacryloyl
chloride, tris(trimethylsilyl)phosphite, and glutamine from Sigma
(Rehovot, Israel); APMA from Polysciences, Inc. (Warrington, PA);
dialysis membrane (1000k—16 mm), sodium carbonate, and sodium
bicarbonate from Bio-Lab Ltd. (Jerusalem, Israel); cyanine7 N-hydroxysuccinimide (Cy7-NHS) ester from Lumiprobe Corporation
(Florida, USA); Dulbecco’s phosphate-buffered saline (PBS),
Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine
serum (FBS), glutamine, and penicillin/streptomycin from Biological
Industries (Beit Haemek, Israel); human osteosarcoma cell line Saos-2
and human colon carcinoma cell line SW620 from American Type Culture
Collection (Manassas, VA); and Matrigel from Sigma (Germany). DDW was purified
by passing deionized DDW through an Elgastat Spectrum reverse osmosis
system (ELGA Ltd., High Wycombe, UK). Coral scaffold was received
as a gift from Boneus Ltd. (Haifa, Israel).
Synthesis of Fluorescent Dye Precursors
Chitosan-PEG Conjugate Synthesis
Leachate characterization and analysis
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