All Photos(3)
Synonym(s):
Lauric acid, NSC 5026
Linear Formula:
CH3(CH2)10COOH
CAS Number:
Molecular Weight:
200.32
Beilstein:
1099477
EC Number:
MDL number:
UNSPSC Code:
12161501
PubChem Substance ID:
NACRES:
NA.77
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Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
WGK
WGK 1
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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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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