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L556

Sigma-Aldrich

Dodecanoic acid

98%

Synonym(s):

ABL, Lauric acid

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About This Item

Linear Formula:
CH3(CH2)10COOH
CAS Number:
143-07-7
Molecular Weight:
200.32
Beilstein/REAXYS Number:
1099477
EC Number:
205-582-1
MDL number:
MFCD00002736
UNSPSC Code:
12352100
PubChem Substance ID:
24896407
NACRES:
NA.22

vapor pressure

1 mmHg ( 121 °C)
50 mmHg ( 210 °C)

Quality Level

200

assay

98%

bp

225 °C/100 mmHg (lit.)

mp

44-46 °C (lit.)

density

0.883 g/mL at 25 °C (lit.)

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

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General description

Dodecanoic acid is a saturated fatty acid used as a starting material or intermediate in the synthesis of pharmaceuticals.

Application

Dodecanoic acid has been used as a reagent to synthesize MnFe2O4 magnetic nanoparticles by seed mediated growth method. It can undergo esterification with 2-ethylhexanol in the presence of sulfated zirconia catalyst to form 2-ethylhexanoldodecanoate, a biodiesel.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

348.8 °F - closed cup

flash_point_c

176 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000356891
0000356891
SHBP7822
SHBP7823
SHBP3361

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Solid Acid Catalysts for Biodiesel Production-Towards Sustainable Energy.
Kiss AA, et al.
advanced synthesis and catalysis, 348(1-2), 75-81 (2006)
Preparation of pyrenyl-based multifunctional nanocomposites for biomedical applications.
Lim EK and Chung BH
Nature Protocols, 11(2), 236-251 (2016)
Isaac Levy et al.
The Journal of clinical endocrinology and metabolism, 100(11), 4106-4113 (2015-09-01)
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There is increasing evidence that both immune and neurochemical alterations are involved in the pathogenesis of bipolar disorder; however, their precise role remains unclear. In this study, we aimed to evaluate neuro-immune changes in a prospective study on children of
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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
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