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L4250

Sigma-Aldrich

Dodecanoic acid

≥99% (GC/titration)

Synonym(s):

Lauric acid, NSC 5026

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About This Item

Linear Formula:
CH3(CH2)10COOH
CAS Number:
143-07-7
Molecular Weight:
200.32
Beilstein:
1099477
EC Number:
205-582-1
MDL number:
MFCD00002736
UNSPSC Code:
12161501
PubChem Substance ID:
24896365
NACRES:
NA.77

Assay

≥99% (GC/titration)

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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Application


  • Biopolymer synthesis for agricultural use: A study engineered Pseudomonas chlororaphis to synthesize biopolymers incorporating 3-hydroxybutyrate and medium-chain-length 3-hydroxyalkanoates from dodecanoic acid. This process highlights its role in sustainable bioplastic production, which could benefit agricultural practices by developing biodegradable mulch films (Deng et al., 2024).

Biochem/physiol Actions

Substrate for CYP 4A11

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

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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Problems derived from obesity and overweight have recently promoted the development of fat substitutes and other low-calorie foods. On the one hand, fats with short- and medium-chain fatty acids are a source of quick energy, easily hydrolyzable and hardly stored
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Careful investigation of the influence of palmitic and lauric acid on the interaction of progesterone and testosterone with several batches of untreated and defatted bovine and human serum albumins have revealed that, by contrast with published data for studies with
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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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