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R7257

Sigma-Aldrich

Acide ricinoléique

≥95%

Synonyme(s) :

Acide ricinélaïdique, Acide (R)-12-hydroxy-cis-9-octadécènoïque, Acide 12-hydroxyoléique

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About This Item

Formule linéaire :
CH3(CH2)5CH(OH)CH2CH=CH(CH2)7COOH
Numéro CAS:
141-22-0
Poids moléculaire :
298.46
Numéro Beilstein :
1727813
Numéro CE :
205-470-2
Numéro MDL:
MFCD00084840
Code UNSPSC :
12352211
ID de substance PubChem :
24899389
Nomenclature NACRES :
NA.25

Source biologique

natural (organic)

Niveau de qualité

200

Pureté

≥95%

Forme

liquid

Densité

0.940 g/mL at 20 °C (lit.)

Groupe fonctionnel

carboxylic acid
hydroxyl

Type de lipide

unsaturated FAs

Conditions d'expédition

ambient

Température de stockage

−20°C

Chaîne SMILES 

CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O

InChI

1S/C18H34O3/c1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21/h9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21)/b12-9-/t17-/m1/s1

Clé InChI

WBHHMMIMDMUBKC-QJWNTBNXSA-N

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Application


  • Multiplexed PLGA scaffolds with nitric oxide-releasing zinc oxide and melatonin-modulated extracellular vesicles for severe chronic kidney disease.: This innovative study utilizes ricinoleic acid in the fabrication of multiplexed PLGA scaffolds, demonstrating its effectiveness in enhancing the therapeutic efficacy of treatments for chronic kidney disease. The research underscores the potential of ricinoleic acid in medical applications, particularly in regenerative medicine and drug delivery systems (Rhim WK et al., 2024).

  • Optimizing the enzymatic production of biolubricants by the Taguchi method: Esterification of the free fatty acids from castor oil with 2-ethyl-1-hexanol catalyzed by Eversa Transform 2.0.: Demonstrates the industrial application of ricinoleic acid in producing biolubricants, emphasizing its economic and environmental benefits. The study provides insights into the sustainable production processes and industrial applications of ricinoleic acid (Monteiro RRC et al., 2024).

Conditionnement

Ampoule scellée.

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

435.2 °F - closed cup

Point d'éclair (°C)

224 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

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DL-β-Hydroxylauric acid ≥99% (GC)

Sigma-Aldrich

H3398

DL-β-Hydroxylauric acid

2-OHOA 2-hydroxyoleic acid (sodium salt), powder

Avanti

791056P

2-OHOA

Castor oil meets testing specifications per USP

Sigma-Aldrich

C9606

Castor oil

Methyl 12-hydroxystearate ≥99% (GC)

Sigma-Aldrich

H7002

Methyl 12-hydroxystearate

Hisashi Yazawa et al.
Applied microbiology and biotechnology, 97(18), 8193-8203 (2013-05-24)
In an effort to produce ricinoleic acid (RA), an important natural raw material with great values as a petrochemical replacement, in Schizosaccharomyces pombe, we introduced Claviceps purpurea oleate Δ12-hydroxylase gene (CpFAH12) to S. pombe, putting it under the control of
Carolin Franzmann et al.
Journal of agricultural and food chemistry, 58(7), 4223-4229 (2010-03-20)
Ergot alkaloid and ricinoleic acid contents of 63 ergot sclerotia samples from rye throughout Germany of the harvest years 2006-2009 were determined. Alkaloid contents were analyzed by means of high-performance liquid chromatography with fluorescence detection (HPLC-FLD) and ricinoleic acid contents
André Arnosti et al.
Experimental parasitology, 127(2), 569-574 (2010-11-13)
This study showed the interference of esters extracted from Ricinus communis in the secretory cycle of salivary glands of Rhipicephalus sanguineus ticks, which consequently caused collateral effects on their feeding process. Ticks attached on hosts which were fed with commercial
Roman Holic et al.
Applied microbiology and biotechnology, 95(1), 179-187 (2012-03-01)
In an effort to produce ricinoleic acid (12-hydroxy-octadeca-cis-9-enoic acid: C18:1-OH) as a petrochemical replacement in a variety of industrial processes, we introduced Claviceps purpurea oleate ∆12-hydroxylase gene (CpFAH12) to Schizosaccharomyces pombe, putting it under the control of inducible nmt1 promoter.
Megan L Robertson et al.
ACS applied materials & interfaces, 3(9), 3402-3410 (2011-08-10)
Poly(l-lactide) (PLLA) is a renewable resource polymer derived from plant sugars with several commercial applications. Broader implementation of the material is limited due to its inherent brittleness. We show that the addition of 5 wt % castor oil to PLLA
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