Castor Oil

Castor Oil

Cat Number
PIE-0409
CAS Number
8001-79-4

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CAS Number
8001-79-4
EINECS
232-293-8
Storage
Room temperature
Synonyms
1,2,3-Propanetriyl (9Z,12R,9Z,12R,9Z,12R)tris(12-hydroxy-9-octadecenoate)
Molecular Formula
C57H104O9
Molecular Weight
933.43
Smiles
O(C(COC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC)C(=O)CCCCCCC\C=C/CC(O)CCCCCC
Appearance
Light yellow sticky liquid
Boiling Point
313 ℃
Standard
USP/EP/CP
General Description
Castor Oil is a colourless to pale-yellow vegetable oil. It is obtained from the seeds of the Ricinus communis plant. Unlike other vegetable oils, Castor oil contains a high percentage of ricinoleic acid, a hydroxylated fatty acid. As such it possesses unique chemical reactivity and lubricating abilities, making it important in manufacturing across several industries such as pharmaceuticals, cosmetics, and industrial synthesis.
Mechanism of Action
Ricinoleic acid is the main active component in Castor Oil, which binds to specific prostanoid receptors. When applied to the skin, it acts as an occlusive humectant that decreases trans-epidermal water loss. Chemically, ricinoleic acid is able to undergo reactions like esterification and ethoxylation due to the hydroxyl groups found in its fatty acid chains. These processes allow manufacturers to produce highly stable surfactants and polymers.
Application
Uses for Castor Oil include serving as a pharmaceutical excipient and solvent medium for lipophilic drugs. It is also used to produce polyoxyethylated castor oil surfactants, which efficiently solubilize insoluble drugs. It is sometimes used in hair and skin care products for conditioning and smoothing effects. Castor Oil is used as a base ingredient in high-performance lubricants, coatings, and biodegradable plastics.

Castor oil-based hybrid microparticles were synthesized for controlled drug release using a green sol-gel technique. Castor oil was modified on a bulk scale with 3-isocyanatopropyltriethoxysilane (IPTES) at 60 ℃ for 30 min under nitrogen. Complete consumption of hydroxyl groups led to silylated triglycerides (ICO). The functionalized oil was emulsified into water (1: 10 w/w) containing thermo-reversible κ-carrageenan or Pluronic F127. Following emulsification using either a four-blade propeller or Ultra-Turrax, the continuous phase was either cooled to 4 ℃ or heated to 60 ℃ to gelate and immobilize the droplets. Ambient moisture over 72 h induced sol-gel condensation of ethoxysilanes. Covalent Si-O-Si networks formed and transitioned liquid droplets into spherical solid particles. The particles were recovered by inversion gelation, washed, centrifuged, and freeze-dried.
Ibuprofen was dissolved within the ICO prior to loading. Loading efficiencies ranged from 55-98%; κ-carrageenan held more drug because pluronic micelles shifted ibuprofen into the external phase. κ-carrageenan-based beads released 100% drug in pH 7.4 buffer at 37 ℃ within 10 h via diffusion. Smaller particles or those based on pluronic show incomplete or biphasic release profiles.

Fig. 1 Castor oil-based hybrid microparticles via a thermo-stabilized o/w emulsion process and sol-gel chemistry. (Gallon G.; <i>et al</i>. 2017) Fig. 1 Castor oil-based hybrid microparticles via a thermo-stabilized o/w emulsion process and sol-gel chemistry. (Gallon G.; et al. 2017)

References

  1. Gallon G.; et al. Cross-linked castor oil-based hybrid microparticles as drug delivery systems. ACS Sustainable Chemistry & Engineering, 2017, 5(5): 4311-4319.

Castor-oil-reinforced polymer hybrid hydrogels were prepared via three freeze-thaw cycles for skin-tissue augmentation by Muzammil K M et al. Chitosan was mixed separately with sodium CMC, HPMC, carbopol or Pluronic F68, followed by a dispersion of castor-oil emulsion. These mixtures were frozen at −20 ℃ and thawed at 25 ℃. FTIR indicated inter-polymeric hydrogen bonding and formation of polyelectrolyte complexes; SEM showed micro-porous rough surfaces. For wound healing evaluation in rat excision wounds, chitosan-Pluronic hybrid (H4) recorded 93.6% wound closure at day 12 with better results than a commercial povidone-iodine standard. Histopathology studies at day 12 showed enhanced re-epithelialisation with dense granulation tissue as well as the presence of abundant neovessels. These hybrids were found to be non-irritant and provided a moist environment with antibacterial characteristics and enhanced keratinocyte and fibroblast proliferation.

Fig. 2 Castor oil-reinforced polymer hybrid hydrogels for skin-tissue augmentation. (Muzammil K M.; <i>et al</i>. 2021) Fig. 2 Castor oil-reinforced polymer hybrid hydrogels for skin-tissue augmentation. (Muzammil K M.; et al. 2021)

References

  1. Muzammil K M.; et al. Castor oil reinforced polymer hybrids for skin tissue augmentation. International Journal of Polymeric Materials and Polymeric Biomaterials, 2021, 70(8): 530-544.

How is Castor Oil different chemically from other oils?

Castor Oil has ricinoleic acid which permits functional hydroxyl groups and unique chemical modifications unavailable in other vegetable oils.

What mechanism of action does Castor Oil have when applied topically?

Castor Oil is a penetrating emollient that attracts moisture to the skin and forms a protective layer over it to help prevent further irritation.

Can Castor Oil be utilized as a drug delivery mechanism?

Yes, Castor Oil is commonly used as a solvent or carrier for hydrophobic active ingredients to increase stability and absorption.

Is there a certificate of analysis or safety data sheet available?

Yes, we include a batch-specific Certificate of Analysis and Safety Data Sheet with every order.

How is Castor Oil used to make surfactants?

Castor Oil can be made into non-ionic surfactants after ethoxylation. These surfactants are commonly used to stabilize emulsions for drug and cosmetic production.
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