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R7257

Sigma-Aldrich

Ricinoleic acid

≥95%

Sinonimo/i:

Ricinelaidic acid, (R)-12-Hydroxy-cis-9-octadecenoic acid, 12-Hydroxyoleic acid

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About This Item

Formula condensata:
CH3(CH2)5CH(OH)CH2CH=CH(CH2)7COOH
Numero CAS:
141-22-0
Peso molecolare:
298.46
Beilstein:
1727813
Numero CE:
205-470-2
Numero MDL:
MFCD00084840
Codice UNSPSC:
12352211
ID PubChem:
24899389
NACRES:
NA.25

Origine biologica

natural (organic)

Saggio

≥95%

Forma fisica

liquid

Densità

0.940 g/mL at 20 °C (lit.)

Gruppo funzionale

carboxylic acid
hydroxyl

Tipo di lipide

unsaturated FAs

Condizioni di spedizione

ambient

Temperatura di conservazione

−20°C

Stringa SMILE

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
WBHHMMIMDMUBKC-QJWNTBNXSA-N

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Applicazioni


  • 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).

Confezionamento

Sealed ampule.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

435.2 °F - closed cup

Punto d’infiammabilità (°C)

224 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (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.
Nuanyi Liang et al.
Food research international (Ottawa, Ont.), 134, 109237-109237 (2020-06-11)
This study investigated the relationships between the structures of hydroxy unsaturated fatty acids (HUFA) and their antifungal activities. Structurally diverse HUFA, including four monohydroxy-18:1 isomers, two monohydroxy 18:2 isomers and two monohydroxy 18:2 isomers were extracted from seeds of plants
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