61610
Dodecanoic acid
puriss., ≥99.0% (GC)
Synonym(s):
Lauric acid, NSC 5026
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About This Item
Linear Formula:
CH3(CH2)10COOH
CAS Number:
Molecular Weight:
200.32
EC Number:
205-582-1
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1099477
grade
puriss.
assay
≥99.0% (GC)
mp
43-46 °C
SMILES string
CCCCCCCCCCCC(O)=O
InChI
1S/C12H24O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)
InChI key
POULHZVOKOAJMA-UHFFFAOYSA-N
Biochem/physiol Actions
Substrate for CYP 4A11
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
348.8 °F - closed cup
flash_point_c
176 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Smritilekha Bera et al.
Journal of medicinal chemistry, 51(19), 6160-6164 (2008-09-10)
Aminoglycoside antibiotics and cationic detergents constitute two classes of clinically important drugs and antiseptics. Their bacteriological and clinical efficacy, however, has decreased recently due to antibiotic resistance. We have synthesized aminoglycoside-lipid conjugates in which the aminoglycoside neomycin forms the cationic
Bhadreshkumar B Maisuria et al.
Bioorganic & medicinal chemistry, 19(9), 2918-2926 (2011-04-16)
Homologous dicarboxyl dendritic amphiphiles-RCONHC(CH(3))(CH(2)CH(2)COOH)(2), 4(n); and ROCONHC(CH(3))(CH(2)CH(2)COOH)(2), 5(n), where R=n-C(n)H(2)(n)(+1) and n=13-22 carbon atoms-were synthesized. Critical micelle concentrations (CMCs) in aqueous triethanolamine solutions and at pH 7.4 were measured along with hemolytic activity (effective concentrations, EC(10)) in phosphate-buffered saline (PBS).
Fu-Chi Chen et al.
Journal of natural products, 68(9), 1318-1323 (2005-09-27)
Five new compounds, kotolactone A (1), kotolactone B (2), secokotomolide (3), kotodiol (4), and 2-acetyl-5-dodecylfuran (5), and 36 known compounds have been isolated from the stem wood of Cinnamomum kotoense. The structures of these new compounds were determined by means