scholarly journals Effect of ricinoleic acid esters from castor oil (Ricinus communis) on the oocyte yolk components of the tick Rhipicephalus sanguineus (Latreille, 1806) (Acari: Ixodidae)

2013 ◽  
Vol 191 (3-4) ◽  
pp. 315-322 ◽  
Author(s):  
Bruno Rodrigues Sampieri ◽  
André Arnosti ◽  
Karim Christina Scopinho Furquim ◽  
Gilberto Orivaldo Chierice ◽  
Gervásio Henrique Bechara ◽  
...  
2011 ◽  
Vol 127 (2) ◽  
pp. 575-580 ◽  
Author(s):  
André Arnosti ◽  
Paula Desjardins Brienza ◽  
Karim Christina Scopinho Furquim ◽  
Gilberto Orivaldo Chierice ◽  
Gervásio Henrique Bechara ◽  
...  

2011 ◽  
Vol 75 (5) ◽  
pp. 683-690 ◽  
Author(s):  
Bruno Rodrigues Sampieri ◽  
André Arnosti ◽  
Pablo Henrique Nunes ◽  
Karim Christina Scopinho Furquim ◽  
Gilberto Orivaldo Chierice ◽  
...  

2012 ◽  
Vol 21 (4) ◽  
pp. 566-576 ◽  
Author(s):  
J. Gandra ◽  
P. Nunes Gil ◽  
N. Cônsolo ◽  
E. Gandra ◽  
A. Gobesso

2020 ◽  
Vol 18 (1) ◽  
pp. 7
Author(s):  
Indra G. Pasaribu ◽  
Arry K. Rizky ◽  
Mario C. Gultom ◽  
Retno G. Dewi ◽  
Tirto P. Prakoso ◽  
...  

bstrak. Minyak jarak kaliki (Ricinus communis L.) merupakan salah satu bahan baku terbarukan yang banyak diaplikasikan di berbagai industri kimia. Salah satu dari turunan minyak jarak kaliki yaitu metil 12-hidroksistearat merupakan metil ester yang memiliki manfaat dalam berbagai jenis industri, khususnya industri pelumas. Makalah ini membahas produksi metil 12-hidroksistearat via hidrogenasi ester minyak jarak dalam reaktor mini-pilot. Makalah ini membahas kondisi optimum proses hidrogenasi dari metil ester risinoleat dengan melakukan variasi terhadap tekanan dan temperatur operasi. Tekanan dan temperatur operasi proses hidrogenasi divariasikan pada rentang 2-4 bar dan 150-210℃. Diperoleh produk hidrogenasi metil ester risinoleat dengan konsentrasi massa metil 12-hidroksistearat mencapai 61,28% dan angka iodin 23,84. Peningkatan temperatur dan tekanan operasi meningkatkan konversi metil 12-hidroksistearat dan menurunkan angka iodin. Pada rentang variasi kondisi, kondisi operasi optimum untuk proses ini adalah temperatur 210℃ dan tekanan 4 bar. Penambahan waktu reaksi hidrogenasi selama 3 jam menghasilkan penurunan angka iodin hingga mencapai 9,82 dan bentuk fisik seperti mentega. Kata kunci: angka iodin, hidrogenasi, metil 12-hidroksistearat, metil ester risinoleat, minyak jarak kaliki. Abstract. Production of Methyl 12-Hydroxystearate through the Hydrogenation Process of Castor Oil Esters. Castor oil (Ricinus communis L.) is one of renewable raw materials widely applied in various chemical industries. One of the castor oil derivatives is methyl 12-hydroxistearate, a methyl ester fatty acid which has been applied in various industries especially lubricants industry. This paper discusses the methyl ester production of methyl 12-hydroxystearate from castor oil via hydrogenation of ester of castor oil in a mini-pilot reactor. The purpose of this study is to determine the optimum operating condition of the hydrogenation process of the ricinoleic acid methyl ester by varying operating pressure and temperature. The operating pressure and temperature of the hydrogenation process were varied in the range of 2-4 bar and 150-210℃. The experimental results show that the hydrogenation process of ricinoleic acid methyl ester produces methyl-12-hydroxistearate with concentration up to 61.28%-wt and Iodine Value of 23.84. Higher operating temperature and pressure increase the conversion of methyl 12- hydroxistearate and reduce the iodine value. Further, the optimum operation condition for this process is at 210℃ and 4 bar. Increasing reaction time for about 3 hours results in a significant reduction of iodine value up to 9.82. Keywords: castor oil, hydrogenation, iodine number, methyl 12-hidroxystearate, methyl ester ricinoleic. Graphical Abstract


2012 ◽  
Vol 112 (2) ◽  
pp. 611-619 ◽  
Author(s):  
B. R. Sampieri ◽  
K. C. S. Furquim ◽  
P. H. Nunes ◽  
M. I. Camargo-Mathias

2019 ◽  
Vol 20 (1) ◽  
pp. 237
Author(s):  
Mohammad Haniff Ahmad ◽  
Wan Asma Ibrahim ◽  
Jahirah Sazali ◽  
Izirwan Izhab ◽  
Zulkafli Hassan

Castor oil is an oil derived from castor seed from a plant Ricinus communis. The versatility of castor oil is highly attributed by 12-hydroxy-9-octadecenoic acid (ricinoleic acid) and its functional group. It is an oil that cannot be consumed by a human. However, castor oil actually can be used to produce many valuable products such as chemicals, paint, and cosmetics due to its unique characteristic which contains a high percentage of ricinoleic acid that helps in producing many valuable products. The utilization of vegetable oils is currently in the highlight of the chemical industry, as they are one of the most important renewable resources due to their universal availability, inherent biodegradability, low price, and eco-friendly. Therefore, the main aim of this paper is to focus on the thermal cracking of castor oil with Zeolite ZSM-5 as the catalyst generates products consisting alcohol, methyl esters and fatty acids which are valuable raw materials for industries. The background, characteristics, composition, properties and industrial application of castor oil have also been discussed. The important properties and various applications of castor oil which can be obtained from toxic seeds have much greater potential than other available vegetable oils.


2007 ◽  
Vol 26 (3_suppl) ◽  
pp. 31-77 ◽  

The oil derived from the seed of the Ricinus communis plant and its primary constituent, Ricinoleic Acid, along with certain of its salts and esters function primarily as skin-conditioning agents, emulsion stabilizers, and surfactants in cosmetics, although other functions are described. Ricinus Communis (Castor) Seed Oil is the naming convention for castor oil used in cosmetics. It is produced by cold pressing the seeds and subsequent clarification of the oil by heat. Castor oil does not contain ricin because ricin does not partition into the oil. Castor oil and Glyceryl Ricinoleate absorb ultraviolet (UV) light, with a maximum absorbance at 270 nm. Castor oil and Hydrogenated Castor Oil reportedly were used in 769 and 202 cosmetic products, respectively, in 2002; fewer uses were reported for the other ingredients in this group. The highest reported use concentration (81%) for castor oil is associated with lipstick. Castor oil is classified by Food and Drug Administration (FDA) as generally recognized as safe and effective for use as a stimulant laxative. The Joint Food and Agriculture Organization (FAO)/World Health Organization (WHO) Expert Committee on Food Additives established an acceptable daily castor oil intake (for man) of 0 to 0.7 mg/kg body weight. Castor oil is hydrolyzed in the small intestine by pancreatic enzymes, leading to the release of glycerol and Ricinoleic Acid, although 3,6-epoxyoctanedioic acid, 3,6-epoxydecanedioic acid, and 3,6-epoxydodecanedioic acid also appear to be metabolites. Castor oil and Ricinoleic Acid can enhance the transdermal penetration of other chemicals. Although chemically similar to prostaglandin E1 , Ricinoleic Acid did not have the same physiological properties. These ingredients are not acute toxicants, and a National Toxicology Program (NTP) subchronic oral toxicity study using castor oil at concentrations up to 10% in the diet of rats was not toxic. Other subchronic studies of castor oil produced similar findings. Undiluted castor oil produced minimal ocular toxicity in one study, but none in another. Undiluted castor oil was severely irritating to rabbit skin in one study, only slightly irritating in another, mildly irritating to guinea pig and rat skin, but not irritating to miniature swine skin. Ricinoleic Acid was nonirritating in mice and in one rabbit study, but produced welldefined erythema at abraded and intact skin sites in another rabbit study. Zinc Ricinoleate was not a sensitizer in guinea pigs. Neither castor oil nor Sodium Ricinoleate was genotoxic in bacterial or mammalian test systems. Ricinoleic Acid produced no neoplasms or hyperplasia in one mouse study and was not a tumor promoter in another mouse study, but did produce epidermal hyperplasia. Castor oil extract had a strong suppressive effect on S180 body tumors and ARS ascites cancer in male Kunming mice. No dose-related reproductive toxicity was found in mice fed up to 10% castor oil for 13 weeks. Female rats injected intramuscularly with castor oil on the first day after estrus had suppressed ovarian folliculogenesis and anti-implantation and abortive effects. Castor oil used as a vehicle control in rats receiving subcutaneous injections had no effect on spermatogenesis. A methanol extract of Ricinus communis var. minor seeds (ether-soluble fraction) produced anti-implantation, anticonceptive, and estrogenic activity in rats and mice. Clinically, castor oil has been used to stimulate labor. Castor oil is not a significant skin irritant, sensitizer, or photosensitizer in human clinical tests, but patients with occupational dermatoses may have a positive reaction to castor oil or Ricinoleic Acid. The instillation of a castor oil solution into the eyes of nine patients resulted in mild and transient discomfort and minor epithelial changes. In another study involving 100 patients, the instillation of castor oil produced corneal epithelial cell death and continuity breaks in the epithelium. Because castor oil contains Ricinoleic Acid as the primary fatty acid group, the Cosmetic Ingredient Review (CIR) Expert Panel considered the safety test data on the oil broadly applicable to this entire group of cosmetic ingredients. The available data demonstrate few toxic effects. Although animal studies indicate no significant irritant or sensitization potential, positive reactions to Ricinoleic Acid in selected populations with identified dermatoses did suggest that sensitization reactions may be higher in that population. Overall, however, the clinical experience suggests that sensitization reactions are seen infrequently. In the absence of inhalation toxicity data on these ingredients, the Panel determined that these ingredients can be used safely in aerosolized cosmetic products because the particle sizes produced are not respirable. Overall, the CIR Expert Panel concluded that these cosmetic ingredients are safe in the practices of use and concentrations as described in this safety assessment.


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