213721
1,2-Dodecanediol
90%
Synonym(s):
1,2-Dihydroxydodecane, 1,2-Dodecylene glycol, 2-Hydroxylauryl alcohol, n-Dodecane-1,2-diol
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About This Item
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Quality Level
Assay
90%
mp
56-60 °C (lit.)
functional group
hydroxyl
SMILES string
CCCCCCCCCCC(O)CO
InChI
1S/C12H26O2/c1-2-3-4-5-6-7-8-9-10-12(14)11-13/h12-14H,2-11H2,1H3
InChI key
ZITKDVFRMRXIJQ-UHFFFAOYSA-N
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Application
1,2-Dodecanediol was used in the preparation of:
- lipophilic diamines and amino alcohols
- Fe(II), Co(II) and Ni(II) ferrite nanoparticles in the range of 9-25 nm
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Memorias do Instituto Oswaldo Cruz, 104(5), 703-705 (2009-10-13)
A series of diamines and amino alcohols derived from 1-dodecanol, 1-tetradecanol, 1,2-dodecanediol and 1,2-tetradecanediol were synthesized and tested for their antitubercular activity. Compounds 3, 8 and 9 were found to be the most active (MIC of 6.25 microg/mL). Nine other
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We synthesized magnetic spinel ferrites from trimetallic single-source precursors. Fe(II), Co(II), and Ni(II) ferrite nanoparticles in the range of 9-25 nm were synthesized by solvothermal decomposition of trimetallic acetate complex precursors in benzyl ether in the presence of oleic acid
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