Monostearin
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Monostearin
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CAS No:
31566-31-1
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Formula:
C21H42O4
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Chemical Name:
Monostearin
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Synonyms:
Octadecanoic acid,monoester with 1,2,3-propanetriol;Stearin,mono-;Monoglyceryl stearate;Glycerol monostearate;Monostearin;Kao Atorum P 40S;Glyceryl monostearate;Glycerin monostearate;Imwitor 191;Nikkol MGS-A;Sinnoester SG;Vykamol S/E;Vykamol N/E;Advawax 140;Myvaplex;Hallmark GMS;Stearic acid glycerol monoester;Rikemal S 100;Nikkol MGS;Imwitor 960K;GMS (glyceride);Stearic acid monoglyceride;Glycerol monooctadecanoate;GMS 90;Aldo SMV;Imwitor 900K;Monogly MB;Aldo MS;Cerasynt SD;Electrostripper TS 5;GMS;Polynol A;Rikemal RMS 100;Aldo 28;Empilan GMS-SE 40;Loxiol G 12;R 60 (glyceride);R 60;Empilan GMS/NSE 40;Cithrol GMS;Rikemal S 100A;KPL 1;Cutina GMS;Rewomul MG;Hostalub FE 2;Atmer 129;CPH 53N;Nissan Monogly MB;Nissan Monogly;Nikkol MGS-ASE;Cerasynt 945;S 100A;Capmul GMS 40;Drewmulse GMS-AE;Brian M 1;Stearic monoglyceride;Poem S 100V;Dimodan PM;Dur-Em 117;Myvaplex 600;Rheodol MS 50;Excel 124;Cerasynt Q;Sunsoft 8000;Rikemal 100;Glycolube 825;Estol 1463;Lipo GMS 470;Rheodol MS 60;TB 123;Denon 2068;Atmer 128;Pelemol GS;Myvaplex 600P;Imwitor 960;Anstex MG 100;Loxiol EP 12;Rikemal 100A;MB 400;S 100;Glycerine monostearate;Cerasynt GMS;Atmer 126;Monogly D;Alkamuls GMS-C;MGS-B;Pationic 902;Pationic 901;Edenor GMS;Nikkol MGS-F 20;Citomulgan T00-785;Citomulgan TOO-785;Myverol 18-06K;Emalsy MH;Radiasurf 7140/3;Sorbon MG 100;Kessco GMS Pure;TS 5;Nissan Monogly 5;Monogly 5;Nikkol MGS-F 50;TG-C;1319-95-5;8029-22-9;8039-58-5;8045-31-6;8050-92-8;12676-39-0;37297-05-5;55962-68-0;58615-57-9;61163-94-8;64366-44-5;69073-02-5;86904-15-6;87714-32-7;100041-47-2;109767-98-8;110618-11-6;119758-60-0;146586-29-0;150605-03-1;176365-67-6;177645-80-6;200138-94-9;209533-94-8;413576-89-3;696587-54-9;902145-16-8;1361318-46-8;1617532-55-4;2025308-77-2
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CAS No:
Description
ChEBI: A rac-1-monoacylglycerol composed of equal amounts of 3-stearoyl-sn-glycerol and 1-stearoyl-sn-glycerol.Monostearin (also known as 1-Stearoyl-rac-glycerol) is a long chain molecule typically occurring in the body as a by-product of the breakdown of fats. It is one of the panels of serum metabolic biomarkers for detecting and diagnosing cancer, especial ovarian cancer. It is also used in the development of drug delivery vehicles such as nanoparticles and microemulsions. It can also be
Characteristics
66.76
5.1443
Colorless, odorless, and sweet flaky powder
1.03 g/cm3 @ Temp: 20 °C
57 °C
476.9ºC at 760 mmHg
151.9ºC
insoluble in water; soluble in hot oils, organic solvents
-20ºC
Safety Information
1
24/25
P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
H315
Monostearin Use and Manufacturing
1, derived from glycerol and stearic acid esterification. Stearic acid, glycerol and sodium hydroxide were added to the reaction kettle, heated and melted and stirred to obtain nitrogen. Heating at 185 ° C for 7 h, the reaction should be at the end of the pH should be less than 5. Cooling out the material, get glycerol monostearate. Per ton of product consumption of stearin greater than 82kg, glycerol (95% or more) 235kg.
2, direct esterification of stearic acid and glycerol according to 1: (1.2 ~ 1
The reaction was carried out at a temperature of 180 to 250 ° C for 2 to 4 hours. The reaction was cooled to 100 ° C and the catalyst was added to the base. After washing with water, the reaction was carried out with 40% ~ 60% of the product. Esterification of glyceryl stearate and glycerol in the presence of 0.06% to 0.1% Cu (OH) 2, at 170 ~ 240 ℃ reaction 1 ~ 2h, the reaction process through the nitrogen for protection, the reaction by deaeration , Acid and refined, refined with a single ester 40% to 60% of the product. Glycerin saponification of glycidic acid and stearic acid in the four ethyl ammonium iodide catalyzed, at 100 ~ 130 ℃ reaction 30 ~ 70min, the reactants refined with a single ester 80% to 90% of the product. Epichlorohydrin phase transfer catalysis epichlorohydrin and sodium stearate (2: 1, molar ratio) in toluene, in the phase transfer catalyst tetrabutyl ammonium bromide catalyzed, at 90 ~ 110 ℃ reaction 2h The reaction was washed with sodium chloride solution, the organic phase was separated, toluene was removed by distillation and unreacted epichlorohydrin was distilled to obtain glycidyl stearate, which was hydrolyzed with 0.1 mol / L NaOH solution, separated and dried , With n-hexane recrystallization products, single ester content of 90% or more. Content of 40% to 60% of the monoester products by molecular distillation can be more than 90% of the high concentration of products.
1. Lonzest(R) GMS is a surfactant used in a variety of markets.
2. Aldo(R) MS BO KFG is a glycerol ester made from soybean oil derived fatty acid. This product finds uses in both food and cosmetic applications.
3. Aldo(R) MSD KFG is a self emulsifying nonionic surfactant, used as a lubricant in confectionery, as a release agent and as a dough softener. It is used as a low HLB emulsifier in personal care products where non animal grade products are needed.
Drug Function and Efficacy
This product is a broad-spectrum antifungal drug that can highly selectively inhibit fungal squalene epoxidase, block the squalene epoxidation reaction during the formation of fungal cell membranes and interfere with the early biosynthesis of fungal sterols, thereby exerting the effect of inhibiting and killing fungi.
Registered Holders
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KERRY Ingredients TRADING(Shanghai) Co., Ltd.
Active
China
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Jiangxi Yipusheng Pharmaceutical Co., Ltd.
Active
China
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Jiangxi Alpha Hi-tech Pharmaceutical Co., Ltd.
Active
China
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