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Key Documents

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:
Molecular Weight:
200.32
Beilstein:
1099477
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

1 mmHg ( 121 °C)
50 mmHg ( 210 °C)

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

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

348.8 °F - closed cup

Flash Point(C)

176 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Solid Acid Catalysts for Biodiesel Production-Towards Sustainable Energy.
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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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