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oleyl alcohol  (Tokyo Chemical Industry)

 
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    Tokyo Chemical Industry oleyl alcohol
    Oleyl Alcohol, supplied by Tokyo Chemical Industry, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/oleyl+alcohol/alcohol+oleyl/pmc13042548-221-26-32
    Average 86 stars, based on 1 article reviews
    oleyl alcohol - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    Methylation:

    Article Title: Thermoplastic polyester resin, thermoplastic polyester resin composition and molded article
    Article Snippet: Raw Materials Terephthalic acid: one manufactured by Mitsui Chemicals, Inc. Dimethyl terephthalate: one manufactured by SK Chemicals Co., Ltd. Isophthalic acid: one manufactured by Tokyo Chemical Industry Co., Ltd. Butanediol: one manufactured by Mitsubishi Chemical Corp. .. Ethylene glycol: one manufactured by Mitsubishi Chemical Corp. Cyclohexanedimethanol: one manufactured by Tokyo Chemical Industry Co., Ltd. Benzoic acid: one manufactured by Tokyo Chemical Industry Co., Ltd. 1-Dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 12 1-Octadecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 1-Docosanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 22 1-Butyloctanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 12 2-Hexyl-1-dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 2-Octyl-1-dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 20 2-Decyl-1-tetradecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 24 2-Dodecyl-1-hexadecanol: ISOFOL 28 manufactured by Sasol Ltd.; carbon number: 28 2-Tetradecyl-1-octadecanol: ISOFOL32 manufactured by Sasol Ltd.; carbon number: 32 Oleyl alcohol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 1-Octadecanoic acid: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 Butanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 4 Octanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 8 2-Ethyl-1-hexanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 8 MPEG: one-end methylated polyethylene glycol having a molecular weight of 550, manufactured by Tokyo Chemical Industry Co., Ltd. Tetrabutyl titanate: one manufactured by Tokyo Chemical Industry Co., Ltd. Magnesium acetate tetrahydrate: one manufactured by Tokyo Chemical Industry Co., Ltd. Antimony trioxide: one manufactured by NIHON SEIKO CO., LTD. Trimethyl phosphate: one manufactured by Tokyo Chemical Industry Co., Ltd. Thermoplastic Resin (B) (B-1) Linear low-density polyethylene resin: “ULTZEX” (registered trademark) 4570 (having a dielectric loss tangent at 5.8 GHz of 0.0009), manufactured by Prime Polymer Co., Ltd. was used. (B-2) Polystyrene resin: GPPS HF77 (having a dielectric loss tangent at 5.8 GHz of 0.0013) manufactured by PS Japan Corporation was used. (B-3) Polycarbonate resin: “TARFLON” (registered trademark) A2200 (having a dielectric loss tangent at 5.8 GHz of 0.0049) manufactured by Idemitsu Kosan Co., Ltd. was used. .. Reactive Compound (C) (C-1) Ethylene-glycidyl methacrylate copolymer: “BONDFAST” (registered trademark) BF-2C (functional group concentration: 600 g/eq) having a content ratio of glycidyl methacrylate of 6%, manufactured by Sumitomo Chemical Company, Limited was used. (C-2) Epoxidized product of styrene-butadiene block copolymer: “EPOFRIEND” (registered trademark) AT501 (having a functional group concentration of 1,000 g/eq), manufactured by Daicel Corp. was used. (C-3) Maleic anhydride-denatured polypropylene: “FUSABOND” (registered trademark) P613 (having a functional group concentration of 4,500 g/eq) manufactured by Dow Inc. was used.

    Molecular Weight:

    Article Title: Thermoplastic polyester resin, thermoplastic polyester resin composition and molded article
    Article Snippet: Raw Materials Terephthalic acid: one manufactured by Mitsui Chemicals, Inc. Dimethyl terephthalate: one manufactured by SK Chemicals Co., Ltd. Isophthalic acid: one manufactured by Tokyo Chemical Industry Co., Ltd. Butanediol: one manufactured by Mitsubishi Chemical Corp. .. Ethylene glycol: one manufactured by Mitsubishi Chemical Corp. Cyclohexanedimethanol: one manufactured by Tokyo Chemical Industry Co., Ltd. Benzoic acid: one manufactured by Tokyo Chemical Industry Co., Ltd. 1-Dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 12 1-Octadecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 1-Docosanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 22 1-Butyloctanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 12 2-Hexyl-1-dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 2-Octyl-1-dodecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 20 2-Decyl-1-tetradecanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 24 2-Dodecyl-1-hexadecanol: ISOFOL 28 manufactured by Sasol Ltd.; carbon number: 28 2-Tetradecyl-1-octadecanol: ISOFOL32 manufactured by Sasol Ltd.; carbon number: 32 Oleyl alcohol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 1-Octadecanoic acid: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 18 Butanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 4 Octanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 8 2-Ethyl-1-hexanol: one manufactured by Tokyo Chemical Industry Co., Ltd.; carbon number: 8 MPEG: one-end methylated polyethylene glycol having a molecular weight of 550, manufactured by Tokyo Chemical Industry Co., Ltd. Tetrabutyl titanate: one manufactured by Tokyo Chemical Industry Co., Ltd. Magnesium acetate tetrahydrate: one manufactured by Tokyo Chemical Industry Co., Ltd. Antimony trioxide: one manufactured by NIHON SEIKO CO., LTD. Trimethyl phosphate: one manufactured by Tokyo Chemical Industry Co., Ltd. Thermoplastic Resin (B) (B-1) Linear low-density polyethylene resin: “ULTZEX” (registered trademark) 4570 (having a dielectric loss tangent at 5.8 GHz of 0.0009), manufactured by Prime Polymer Co., Ltd. was used. (B-2) Polystyrene resin: GPPS HF77 (having a dielectric loss tangent at 5.8 GHz of 0.0013) manufactured by PS Japan Corporation was used. (B-3) Polycarbonate resin: “TARFLON” (registered trademark) A2200 (having a dielectric loss tangent at 5.8 GHz of 0.0049) manufactured by Idemitsu Kosan Co., Ltd. was used. .. Reactive Compound (C) (C-1) Ethylene-glycidyl methacrylate copolymer: “BONDFAST” (registered trademark) BF-2C (functional group concentration: 600 g/eq) having a content ratio of glycidyl methacrylate of 6%, manufactured by Sumitomo Chemical Company, Limited was used. (C-2) Epoxidized product of styrene-butadiene block copolymer: “EPOFRIEND” (registered trademark) AT501 (having a functional group concentration of 1,000 g/eq), manufactured by Daicel Corp. was used. (C-3) Maleic anhydride-denatured polypropylene: “FUSABOND” (registered trademark) P613 (having a functional group concentration of 4,500 g/eq) manufactured by Dow Inc. was used.

    Modification:

    Article Title: Modified cellulose nanofiber and rubber composition including the same
    Article Snippet: .. A substituted carboxy group-containing modified cellulose nanofiber was obtained in the same manner as in Production Example 1, except that oleylamine in Production Example 1 was changed to oleyl alcohol (manufactured by Tokyo Chemical Industry Co., Ltd.). ..

    other:

    Article Title: Iron Oxide Nanozyme as Reactive Oxygen and Nitrogen Species Scavenger to Regulate Microglial Homeostasis in Stroke.
    Article Snippet: Ferric chloride hexahydrate ( > 99%), sodium oleate were purchased from Sinopharm Chemical Reagent Co., Ltd. Oleic acid, benzyl ether, 1-octadecene and were purchased from Sigma– ldrich Co ., Ltd. Oleyl alcohol (65.0%) were purchased from TCI Co., Ltd.

    Article Title: An electro-ferroptotic nanoammunition enables image-guided, spatiotemporally controlled cancer ferroptosis induction via irreversible electroporation
    Article Snippet: Ferroptosis, an iron-dependent regulated cell death pathway, has emerged as a promising modality for cancer therapy.. However, current iron-based ferroptosis inducers, which trigger the Fenton reaction and release Fe2+, face challenges associated with limited cytosolic Fe2+ accumulation, leading to suboptimal ferroptosis induction.. Herein, we report an electro-ferroptotic nanoammunition (EFN) composed of iron oxide nanoassembly (IONA) and ascorbic acid-loaded liposomes (Lip-AA) that enables image-guided, spatiotemporally controlled ferroptosis induction via irreversible electroporation (IRE) for enhanced cancer ferroptotic therapy.

    Article Title: Synergistic regulation of longitudinal and transverse relaxivity of extremely small iron oxide nanoparticles (ESIONPs) using pH-responsive nanoassemblies.
    Article Snippet: Extremely small iron oxide nanoparticles (ESIONPs), as a kind of the special T1 magnetic resonance imaging (MRI) contrast agent that can provide T1 contrasting enhancement since their magnetically disordered shells are dominant compared to their magnetic cores and have powerful potential for constructing stimuli-responsive contrast agents (CAs) to realize precise the tumor diagnosis with high specificity and sensitivity.. The stimuli-responsive function of ESIONPs-based CAs can be directly endowed through the synergistic regulation of the longitudinal and transverse relaxivity (r1 and r2) of ESIONPs.. However, the systematical investigation for the synergistic regulation of r1 and r2 of ESIONPs is quite lacking.

    Article Title: Iron Oxide Nanozyme as Reactive Oxygen and Nitrogen Species Scavenger to Regulate Microglial Homeostasis in Stroke
    Article Snippet: Ferric chloride hexahydrate (>99%), sodium oleate were purchased from Sinopharm Chemical Reagent Co., Ltd. Oleic acid, benzyl ether, 1‐octadecene and were purchased from Sigma–Aldrich Co., Ltd. Oleyl alcohol (65.0%) were purchased from TCI Co., Ltd.



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    Low temperature esterification of Fe( ii ) oleate for synthesis of iron oxide nanoparticles at 290 °C and a precursor addition rate of 0.1 mmol min −1 yields particles that are too small to be effective MPI tracers. (A) Fourier Transform Infrared (FTIR) facilitates tracking of reaction progress, as the main peaks for the reagents (iron oleate and <t>oleyl</t> <t>alcohol)</t> and the ester product can be obtained from reaction aliquots. (B) Tracking FTIR intensity over reaction time demonstrates ester formation (yellow) and alcohol consumption (teal) in region (i) with the addition of 6 mmol of Fe. Further addition, results in iron oleate (brown) accumulation due to the alcohol depletion observed in region (ii). (C) Physical size distributions obtained from analysis of transmission electron microscopy (TEM) images show that polydisperse particles of ∼6 nm quickly form after 5 min of reaction and grow to a size of ∼10 nm after 120 min and 12 mmol Fe is added. Scale bars are 20 nm.
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    Low temperature esterification of Fe( ii ) oleate for synthesis of iron oxide nanoparticles at 290 °C and a precursor addition rate of 0.1 mmol min −1 yields particles that are too small to be effective MPI tracers. (A) Fourier Transform Infrared (FTIR) facilitates tracking of reaction progress, as the main peaks for the reagents (iron oleate and <t>oleyl</t> <t>alcohol)</t> and the ester product can be obtained from reaction aliquots. (B) Tracking FTIR intensity over reaction time demonstrates ester formation (yellow) and alcohol consumption (teal) in region (i) with the addition of 6 mmol of Fe. Further addition, results in iron oleate (brown) accumulation due to the alcohol depletion observed in region (ii). (C) Physical size distributions obtained from analysis of transmission electron microscopy (TEM) images show that polydisperse particles of ∼6 nm quickly form after 5 min of reaction and grow to a size of ∼10 nm after 120 min and 12 mmol Fe is added. Scale bars are 20 nm.
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    Image Search Results


    Low temperature esterification of Fe( ii ) oleate for synthesis of iron oxide nanoparticles at 290 °C and a precursor addition rate of 0.1 mmol min −1 yields particles that are too small to be effective MPI tracers. (A) Fourier Transform Infrared (FTIR) facilitates tracking of reaction progress, as the main peaks for the reagents (iron oleate and oleyl alcohol) and the ester product can be obtained from reaction aliquots. (B) Tracking FTIR intensity over reaction time demonstrates ester formation (yellow) and alcohol consumption (teal) in region (i) with the addition of 6 mmol of Fe. Further addition, results in iron oleate (brown) accumulation due to the alcohol depletion observed in region (ii). (C) Physical size distributions obtained from analysis of transmission electron microscopy (TEM) images show that polydisperse particles of ∼6 nm quickly form after 5 min of reaction and grow to a size of ∼10 nm after 120 min and 12 mmol Fe is added. Scale bars are 20 nm.

    Journal: Nanoscale

    Article Title: Esterification synthesis of iron oxide nanoparticle tracers for magnetic particle imaging (MPI)

    doi: 10.1039/d5nr03157e

    Figure Lengend Snippet: Low temperature esterification of Fe( ii ) oleate for synthesis of iron oxide nanoparticles at 290 °C and a precursor addition rate of 0.1 mmol min −1 yields particles that are too small to be effective MPI tracers. (A) Fourier Transform Infrared (FTIR) facilitates tracking of reaction progress, as the main peaks for the reagents (iron oleate and oleyl alcohol) and the ester product can be obtained from reaction aliquots. (B) Tracking FTIR intensity over reaction time demonstrates ester formation (yellow) and alcohol consumption (teal) in region (i) with the addition of 6 mmol of Fe. Further addition, results in iron oleate (brown) accumulation due to the alcohol depletion observed in region (ii). (C) Physical size distributions obtained from analysis of transmission electron microscopy (TEM) images show that polydisperse particles of ∼6 nm quickly form after 5 min of reaction and grow to a size of ∼10 nm after 120 min and 12 mmol Fe is added. Scale bars are 20 nm.

    Article Snippet: Oleyl alcohol (80–85% technical grade), hexane (>98.5%, certified ACS), toluene (>99.5%, certified ACS), ethanol (200 proof), and tetrahydrofuran (THF, 99.8% for HPLC) were purchased from Thermo Fisher Scientific (Waltham, MA).

    Techniques: Fourier Transform Infrared Spectroscopy, Transmission Assay, Electron Microscopy