WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H111509
CAS#: 112-53-8
Description: 1-Dodecanol is a saturated fatty alcohol from coconut oil fatty acids. It has a floral odor and is used in detergents, Lepidopteran pheromone/sex attractant, lubricating oils, pesticides and pharmaceuticals.
Hodoodo Cat#: H111509
Name: 1-Dodecanol
CAS#: 112-53-8
Chemical Formula: C12H26O
Exact Mass: 186.20
Molecular Weight: 186.340
Elemental Analysis: C, 77.35; H, 14.06; O, 8.59
Synonym: AI3-00309, AI3 00309, AI300309, Alcohol C-12, Alfol 12, C12 alcohol, CCRIS 662, HSDB 1075, HSDB1075, HSDB-1075, Lauric alcohol, Laurinic alcohol, Lauroyl alcohol, Lauryl alcohol, NAA 42, Nacol 12-96, NSC 3724, NSC3724, NSC-3724, Pisol,
IUPAC/Chemical Name: dodecan-1-ol
InChi Key: LQZZUXJYWNFBMV-UHFFFAOYSA-N
InChi Code: InChI=1S/C12H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2-12H2,1H3
SMILES Code: CCCCCCCCCCCCO
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: To be determined
Shelf Life: >2 years if stored properly
Drug Formulation: To be determined
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
More Info:
Biological target: | |
In vitro activity: | |
In vivo activity: |
The following data is based on the product molecular weight 186.34 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
Formulation protocol: | |
In vitro protocol: | |
In vivo protocol: |
1: Lee Y, Jung SW, Park SH, Yoo JW, Park J. Synthesis of Tungsten-Doped Vanadium
Dioxide Using a Modified Polyol Method Involving 1-Dodecanol. Materials (Basel).
2020 Nov 27;13(23):5384. doi: 10.3390/ma13235384. PMID: 33260827; PMCID:
PMC7730659.
2: Ananiadou A, Papamokos G, Steinhart M, Floudas G. Nanometer Confinement
Induces Nematic Order in 1-Dodecanol. J Phys Chem B. 2020 Nov
25;124(47):10850-10857. doi: 10.1021/acs.jpcb.0c08403. Epub 2020 Nov 13. PMID:
33185090.
3: Çetinkaya S. A Novel Isolate (S15) of Streptomyces griseobrunneus Produces
1-Dodecanol. Curr Microbiol. 2021 Jan;78(1):144-149. doi:
10.1007/s00284-020-02261-3. Epub 2020 Oct 29. PMID: 33123751.
4: Tian Z, Li Y, Zhou T, Ye X, Li R, Liu J. Structure dynamics reveal key
residues essential for the sense of 1-dodecanol by Cydia pomonella pheromone
binding protein 2 (CpomPBP2). Pest Manag Sci. 2020 Nov;76(11):3667-3675. doi:
10.1002/ps.5915. Epub 2020 Jun 20. PMID: 32418321.
5: Yao MM, Jiang CH, Yao JS, Wang KH, Chen C, Yin YC, Zhu BS, Chen T, Yao HB.
General Synthesis of Lead-Free Metal Halide Perovskite Colloidal Nanocrystals in
1-Dodecanol. Inorg Chem. 2019 Sep 3;58(17):11807-11818. doi:
10.1021/acs.inorgchem.9b01893. Epub 2019 Aug 9. PMID: 31398054.
6: Yamaguchi T, Faraone A, Nagao M. Collective Mesoscale Dynamics of Liquid
1-Dodecanol Studied by Neutron Spin-Echo Spectroscopy with Isotopic Substitution
and Molecular Dynamics Simulation. J Phys Chem B. 2019 Jan 10;123(1):239-246.
doi: 10.1021/acs.jpcb.8b10299. Epub 2018 Dec 20. PMID: 30511874.
7: Hsieh SC, Wang JH, Lai YC, Su CY, Lee KT. Production of 1-Dodecanol,
1-Tetradecanol, and 1,12-Dodecanediol through Whole-Cell Biotransformation in
Escherichia coli. Appl Environ Microbiol. 2018 Jan 31;84(4):e01806-17. doi:
10.1128/AEM.01806-17. PMID: 29180361; PMCID: PMC5795085.
8: Flavel BS, Kappes MM, Krupke R, Hennrich F. Separation of single-walled
carbon nanotubes by 1-dodecanol-mediated size-exclusion chromatography. ACS
Nano. 2013 Apr 23;7(4):3557-64. doi: 10.1021/nn4004956. Epub 2013 Apr 5. PMID:
23540203.
9: Tanaka S, Tashiro Y, Kobayashi G, Ikegami T, Negishi H, Sakaki K. Membrane-
assisted extractive butanol fermentation by Clostridium
saccharoperbutylacetonicum N1-4 with 1-dodecanol as the extractant. Bioresour
Technol. 2012 Jul;116:448-52. doi: 10.1016/j.biortech.2012.03.096. Epub 2012 Apr
4. PMID: 22575842.
10: Domínguez H. Structure of the SDS/1-dodecanol surfactant mixture on a
graphite surface: a computer simulation study. J Colloid Interface Sci. 2010 May
15;345(2):293-301. doi: 10.1016/j.jcis.2010.02.062. Epub 2010 Mar 3. PMID:
20303501.
11: Cueto GM, Zerba E, Picollo MI. Biological effect of 1-dodecanol in teneral
and post-teneral Rhodnius prolixus and Triatoma infestans (Hemiptera:
Reduviidae). Mem Inst Oswaldo Cruz. 2005 Feb;100(1):59-61. doi:
10.1590/s0074-02762005000100012. Epub 2005 Apr 12. PMID: 15867966.
12: Miura Y. Omega- and (omega-1)-hydroxylation of 1-dodecanol by frog liver
microsomes. Lipids. 1981 Oct;16(10):721-5. doi: 10.1007/BF02535338. PMID:
6975411.