Ricinus communis Root Extract is a plant powder obtained by various extraction methods (chemical or solvent extraction using n-hexane and supercritical carbon dioxide, aqueous and reactive enzymes accompanied by ultrasound, triethyl citrate, Indole-3-acetic acid ) from the seeds of Ricinus communis L., an annual herbaceous plant belonging to the Euphorbiaceae family. It is composed of ricinoleic acid, a hydroxylated fatty acid, carotenoids, tocopherols and other interesting constituents.
It appears in the form of a brown powder. It can be mixed with ethanol, chloroform, diethylether, acetic acid and methanol.
What it is used for and where
Cosmetics
Fragrance. It plays a very important role in the formulation of cosmetic products as it allows perfume to be enhanced, masked or added to the final product, improving its commercial viability. The consumer always expects to find a pleasant scent in a cosmetic product.
In powder form can be hydrogenated and is an emulsifying agent.
Some information on castor oil, the most widespread derivative of the panta Ricinus communis.
Insecticides
Castor oil has shown some potential in the practical control of both immature and adult stages of the mosquito vector, particularly against the important dengue vector, Aedes aegypti, and has been tested for macrophilicidal activity against adults of Setaria digitata a parasitic nematode found in the peritoneal cavity of cattle. The toxicity of methanol, ethyl acetate, chloroform and petroleum ether extracts of the leaf of R. communis was tested against third stage Musca domestica larvae (Singh & Kaur, 2016). Crude methane extracts of R. communis leaves showed moderate acaricidal and insecticidal activity against Haemaphysalis bispinosa and Hippobosca maculate (Zahir et al., 2010a) (3).
Medical
Castor oil has been used by traditional medical science as a purgative and as a method of initiating labour in obstetrical practice. Ricinus communis contains 80-90% ricinoleic acid and, among other applications, is used as a co-polyester of ricinoleic-lactic acid as a drug carrier (1) and has demonstrated anti-inflammatory, bactericidal and anti-herpetic properties (2).
Other Uses
Used to produce polyurethane coatings, rubber, dicarboxylic acid, plasticisers and various types of oil such as insulating oil, Turkish red oil, hydraulic oil. It is also used to produce polyamide-11 fibre and soap.
In the leather industry it serves as a greasing agent, extender and bleaching agent for finishing.
In the textile industry it is a penetrating and emulsifying agent.
When dehydrated, a conjugated dry double bond oil is obtained.
Safety
In 2007, the CIR (Cosmetic Ingredient Review) Expert Group suggested that sensitisation reactions were rarely observed and this ingredient can be used safely in cosmetic products even when aerosolised because the particle sizes produced are not respirable. Overall, the CIR Expert Panel concluded that this cosmetic ingredient is safe in the use practices and concentrations described in this safety assessment (4).
For more information:
Castor seed oil studies
Typical commercial product characteristics Castor seed oil
Appearance | White powder or colorless or slight yellow liquid |
Boiling Point
| 879.2±65.0°C at 760 mmHg |
Melting Point | -12ºC |
Flash Point | 224.1±27.8°C |
Freezing Point
| -10℃ |
Density | 1.0±0.1 g/cm3 |
Relative density | 0.956 ~ 0.969 |
Refraction Index | 1.490 |
Vapor Pressure
| 0.0±0.6 mmHg at 25°C |
PSA | 139.59000 |
LogP | 17.72 |
Water Solubility
| <0.1 g/100 mL at 20 ºC |
Refractive Rate | n20/D1.478(lit.) |
Autogenous Ignition | 449°C (liquid) |
Relative density | 0.956 ~ 0.969 (liquid) |
Shelf Life | 24 months |
- Molecular Formula C57H104O9
- Molecular Weight 933.4
- Exact Mass 932.768005
- CAS 8001-79-4
- UNII D5340Y2I9G
- EC Number 232-293-8
- DSSTox Substance ID DTXSID7024742
- IUPAC 2,3-bis[[(Z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (Z)-12-hydroxyoctadec-9-enoate
- InChl=1S/C57H104O9/c1-4-7-10-31-40-51(58)43-34-25-19-13-16-22-28-37-46-55(61)64-49-54(66-57(63)48-39-30-24-18-15-21-27-36-45-53(60)42-33-12-9-6-3)50-65-56(62)47-38-29-23-17-14-20-26-35-44-52(59)41-32-11-8-5-2/h25-27,34-36,51-54,58-60H,4-24,28-33,37-50H2,1-3H3/b34-25-,35-26-,36-27-
- InChl Key ZEMPKEQAKRGZGQ-AAKVHIHISA-N
- SMILES CCCCCCC(CC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC(CCCCCC)O)OC(=O)CCCCCCCC=CCC(CCCCCC)O)O
- MDL number MFCD00130746
- PubChem Substance ID
- RTECS FI4100000 YX1850000
- FEMA 2263
- NCI C80990
- ICSC 1452
Synonyms:
- Ricinus oil
- Castor oil
- Olio di ricino
References_______________________________________________________________________
(1) Slivniak, R.; Ezra, A.; Domb, A.J. Hydrolytic degradation and drug release of ricinoleic acid-lactic acid copolyesters. Pharm. Res. 23, 1306-1312 (2006)
(2) Gamayurova, V.S.; Zinov’Eva, M.E.; Tran, H.T.T. Features of the enzymatic hydrolysis of castor oil. Catal. Ind. 5, 269-273 (2013).
(3) Wamaket N, Dieng H, Komalamisra N, Apiwathnasorn C, Morales RE, Thanomsub BW, Srisawat R, Attrapadung S. Larvicidal and adulticidal activities of castor oil against the dengue vector, Aedes aegypti. Trop Biomed. 2018 Sep 1;35(3):610-618.
(4) Final report on the safety assessment of Ricinus Communis (Castor) Seed Oil, Hydrogenated Castor Oil, Glyceryl Ricinoleate, Glyceryl Ricinoleate SE, Ricinoleic Acid, Potassium Ricinoleate, Sodium Ricinoleate, Zinc Ricinoleate, Cetyl Ricinoleate, Ethyl Ricinoleate, Glycol Ricinoleate, Isopropyl Ricinoleate, Methyl Ricinoleate, and Octyldodecyl Ricinoleate. Int J Toxicol. 2007;26 Suppl 3:31-77. doi: 10.1080/10915810701663150