12-Hydroxystearic acid (CAS 106-14-9)

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12-гидроксистеариновая кислота (12-ГСК/12. CAS 106-14-9.

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Free, and generated automatically from the sources listed on this page. No person has reviewed it, and it describes the substance in general — not your material, your process or your intended market.

REACH 2020/878
v1 · 03.09.2026

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Chemische Übersicht: 12-Hydroxystearic acid
SummenformelC18H36O3
Molekulargewicht300.5 g/mol
LogP (Lipophilie)6.5
IUPAC-Name12-hydroxyoctadecanoic acid
SMILESCCCCCCC(CCCCCCCCCCC(=O)O)O
InChIKeyULQISTXYYBZJSJ-UHFFFAOYSA-N

Synonyme: 12-Hydroxystearic acid · 12-HYDROXYOCTADECANOIC ACID · 106-14-9 · DL-12-Hydroxystearic acid · Cerit Fac 3

Datenquellen: PubChem (NLM/NIH)
Zuletzt aktualisiert: 2026-09-02

WISSENSCHAFTLICHE FORSCHUNG

[1]PubMed2025
Roddy GPT, Manni LS, Atkin R et al.. (2025). "12-Hydroxyoctadecanoic acid forms two kinds of supramolecular gels in nanostructured protic ionic liquids.". Journal of colloid and interface science. htt
[2]CrossRef2024
Yu Duan, Xian-Zhao Liu, En-Nian Li et al.. (2024). "Determination of stearic acid and 12-hydroxyoctadecanoic acid in PEG-60 hydrogenated castor oil by HPLC-ELSD after alkaline hydrolysis". Acta Chroma
[3]Doaj2022
Masar Basim Mohsin Mohamed , Zainab Saad Qaddoori, Ghiadaa Sulaiman Hammed. (2022). "Study the Effect of 12-Hydroxyoctadecanoic Acid Concentration on Preparation and Characterization of Floating Organ
[4]PubMed2018
Steck K, Schmidt C, Stubenrauch C. (2018). "The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water-Surfactant-12-HOA System: Gelator and Co-Surfactant.". Gels (Basel, Switzerland)
[5]PubMed2016
Rogers MA, Marangoni AG. (2016). "Kinetics of 12-Hydroxyoctadecanoic Acid SAFiN Crystallization Rationalized Using Hansen Solubility Parameters.". Langmuir : the ACS journal of surfaces and colloids.
[6]CrossRef2015
Michaela Laupheimer, Natalie Preisig, Cosima Stubenrauch. (2015). "The molecular organogel n-decane/12-hydroxyoctadecanoic acid: Sol–gel transition, rheology, and microstructure". Colloids and Surface
[7]CrossRef2013
Songwei Wu, Jie Gao, Thomas J. Emge et al.. (2013). "Solvent-Induced Polymorphic Nanoscale Transitions for 12-Hydroxyoctadecanoic Acid Molecular Gels". Crystal Growth & Design. https://doi.org/10.1021
[8]CrossRef2010
Hisako Sato, Takara Sakurai, Akihiko Yamagishi. (2010). "Comparison of Vibrational Circular Dichroism between the Langmuir–Blodgett Films and Gels of 12-Hydroxyoctadecanoic Acid". Chemistry Letters. h
📚 Wissenschaftliche Referenzen (Chicago Author-Date) 15 refs · 3 baz

MOLECULE Bibliografie pro CAS (live aus 13+ Datenbanken)

Quellen: db:pubmed (3) · db:crossref (11) · db:doaj (1)

  1. db:pubmed Roddy GPT, Manni LS, Atkin R et al.. (2025). "12-Hydroxyoctadecanoic acid forms two kinds of supramolecular gels in nanostructured protic ionic liquids.". Journal of colloid and interface science. https://doi.org/10.1016/j.jcis.2025.137384
  2. db:crossref Yu Duan, Xian-Zhao Liu, En-Nian Li et al.. (2024). "Determination of stearic acid and 12-hydroxyoctadecanoic acid in PEG-60 hydrogenated castor oil by HPLC-ELSD after alkaline hydrolysis". Acta Chromatographica. https://doi.org/10.1556/1326.2023.01116
  3. db:doaj Masar Basim Mohsin Mohamed , Zainab Saad Qaddoori, Ghiadaa Sulaiman Hammed. (2022). "Study the Effect of 12-Hydroxyoctadecanoic Acid Concentration on Preparation and Characterization of Floating Organogels using Cinnarizin as Modeling Drug". Iraqi Journal of Pharmaceutical Sciences. https://doi.org/10.31351/vol31iss2pp169-176
  4. db:pubmed Steck K, Schmidt C, Stubenrauch C. (2018). "The Twofold Role of 12-Hydroxyoctadecanoic Acid (12-HOA) in a Ternary Water-Surfactant-12-HOA System: Gelator and Co-Surfactant.". Gels (Basel, Switzerland). https://doi.org/10.3390/gels4030078
  5. db:pubmed Rogers MA, Marangoni AG. (2016). "Kinetics of 12-Hydroxyoctadecanoic Acid SAFiN Crystallization Rationalized Using Hansen Solubility Parameters.". Langmuir : the ACS journal of surfaces and colloids. https://doi.org/10.1021/acs.langmuir.6b03476
  6. db:crossref Michaela Laupheimer, Natalie Preisig, Cosima Stubenrauch. (2015). "The molecular organogel n-decane/12-hydroxyoctadecanoic acid: Sol–gel transition, rheology, and microstructure". Colloids and Surfaces A: Physicochemical and Engineering Aspects. https://doi.org/10.1016/j.colsurfa.2015.01.039
  7. db:crossref Songwei Wu, Jie Gao, Thomas J. Emge et al.. (2013). "Solvent-Induced Polymorphic Nanoscale Transitions for 12-Hydroxyoctadecanoic Acid Molecular Gels". Crystal Growth & Design. https://doi.org/10.1021/cg400124e
  8. db:crossref Hisako Sato, Takara Sakurai, Akihiko Yamagishi. (2010). "Comparison of Vibrational Circular Dichroism between the Langmuir–Blodgett Films and Gels of 12-Hydroxyoctadecanoic Acid". Chemistry Letters. https://doi.org/10.1246/cl.2011.25
  9. db:crossref P. Terech, V. Rodriguez, J. D. Barnes et al.. (1994). "Organogels and Aerogels of Racemic and Chiral 12-Hydroxyoctadecanoic Acid". Langmuir. https://doi.org/10.1021/la00022a009
  10. db:crossref Kunio NAGASHIMA, Ikuko YAMADA, Toshiyuki HOBO et al.. (1990). "Chloride ion and nitrate ion selective electrodes using 12-hydroxyoctadecanoic acid matrix.". BUNSEKI KAGAKU. https://doi.org/10.2116/bunsekikagaku.39.11_785
  11. db:crossref Hirosi Matuo, D.K. Rice, D.M. Balthasar et al.. (1982). "Mixed monolayer studies of 12-hydroxyoctadecanoic acid and its esters". Chemistry and Physics of Lipids. https://doi.org/10.1016/0009-3084(82)90030-5
  12. db:crossref Nobuyuki Ito, Masako Yudasaka, Tsunetake Fujiyama. (1981). "Light Scattering Study of the 12-Hydroxyoctadecanoic Acid and Benzene Mixture in the Gel State". Bulletin of the Chemical Society of Japan. https://doi.org/10.1246/bcsj.54.1939
  13. db:crossref Hirosi Matuo, Terumasa Mitsui, Kinsi Motomura et al.. (1981). "Eutectic transformation in mixed monolayers of long normal chain fatty acids with 12-hydroxyoctadecanoic acid". Chemistry and Physics of Lipids. https://doi.org/10.1016/0009-3084(81)90048-7
  14. db:crossref TARO TACHIBANA, TOMOKO MORI, KAYAKO HORI. (1979). "New type of twisted mesophase in jellies and solid films of chiral 12-hydroxyoctadecanoic acid". Nature. https://doi.org/10.1038/278578a0
  15. db:crossref (0). "Kinetics of 12-Hydroxyoctadecanoic Acid SAFiN Crystallization Rationalized Using Hansen Solubility Parameters". https://doi.org/10.1021/acs.langmuir.6b03476.s001
Regulatorischer Status der Substanz
Diese Substanz unterliegt regulatorischen Anforderungen: Bewirtschaftung gefährlicher Abfälle (BDO-Register). Details im Abschnitt "Regulatorischer Status (REACH/ECHA/CLP)" und im SDS. Regulatorische Information — schränkt den Kauf in diesem Shop nicht ein.
🧪 Chemische Daten
CAS-Nummer
106-14-9
Summenformel
C18H36O3
Molmasse
300.5 g/mol
IUPAC-Name (EN)
12-hydroxyoctadecanoic acid
SMILES
CCCCCCC(CCCCCCCCCCC(=O)O)O
InChIKey
ULQISTXYYBZJSJ-UHFFFAOYSA-N
🔍 Externe Identifikatoren
12 von 16 ID-Systemen75%
DatenbankIdentifikatorAktionen
CAS Registry Number106-14-9Öffnen →
PubChem CID7789[1]Öffnen →
InChIKeyULQISTXYYBZJSJ-UHFFFAOYSA-N[1]Öffnen →
InChIInChI=1S/C18H36O3/c1-2-3-4-11-14-17(19)15-12-9-7…[1]
SMILESCCCCCCC(CCCCCCCCCCC(=O)O)O[1]
EC Number203-366-1[2]Öffnen →
ChEMBLCHEMBL292352[3]Öffnen →
HMDBHMDB0061706Öffnen →
ChemSpider7501[4]Öffnen →
UNII (FDA)933ANU3H2SÖffnen →
NSC Number (NCI)2385Öffnen →
WikiData QIDQ10843743Öffnen →

Quellen: PubChem (NIH), Wikidata SPARQL, KEGG, ChEMBL (EBI), CompTox CTX (EPA).

📚 Wissenschaftliche Referenzen (Chicago Author-Date) (4 Quellen)
  1. PubChem. National Center for Biotechnology Information (NIH/NLM), chemical compound database. dotyczy: PubChem CID · InChIKey · InChI · SMILES
  2. ECHA. EC Inventory — EINECS, ELINCS, NLP and List Numbers assigned under REACH. Helsinki: European Chemicals Agency. dotyczy: EC Number
  3. ChEMBL. European Bioinformatics Institute (EMBL-EBI), bioactivity database. dotyczy: ChEMBL
  4. ChemSpider. Royal Society of Chemistry, chemical structure database. dotyczy: ChemSpider

Dalsza literatura

Publications topically related to this CAS. They are not the source of any value given on this card.

Bibliografie (erweitert) (2)

  1. ★★☆☆☆ CROSSREF 🔓 OFFEN ❓ nicht verifiziert Rogers, Michael A.. 2018. "12-Hydroxystearic Acid Oleogels." Edible Oleogels: 85-102. https://doi.org/10.1016/b978-0-12-814270-7.00004-6. Link [abgerufen: 2026-09-03] CC0 (metadata)
  2. ★★☆☆☆ CROSSREF 🔓 OFFEN ❓ nicht verifiziert Anonymous. "Thermal and Rheological Behavior of the Organogelators 12-Hydroxystearic Acid and Its Calcium Salt.". https://doi.org/10.1021/acs.iecr.4c02684.s001. Link [abgerufen: 2026-09-03] CC0 (metadata)

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12-гидроксистеариновая кислота (12-ГСК/12 — CAS 106-14-9. Listed by Uts Shanghai. Prepared from the supplier’s public catalogue; not verified against their internal data.

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