L3253
Propyl dodecanoate
~99%
Synonym(s):
Lauric acid propyl ester, Propyl laurate
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About This Item
Empirical Formula (Hill Notation):
C15H30O2
CAS Number:
Molecular Weight:
242.40
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
assay
~99%
density
0.86 g/mL at 25 °C (lit.)
storage temp.
−20°C
SMILES string
CCCCCCCCCCCC(=O)OCCC
InChI
1S/C15H30O2/c1-3-5-6-7-8-9-10-11-12-13-15(16)17-14-4-2/h3-14H2,1-2H3
InChI key
FTBUKOLPOATXGV-UHFFFAOYSA-N
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Hamid Reza Fard Masoumi et al.
TheScientificWorldJournal, 2013, 962083-962083 (2013-12-11)
Lipase-catalyzed production of triethanolamine-based esterquat by esterification of oleic acid (OA) with triethanolamine (TEA) in n-hexane was performed in 2 L stirred-tank reactor. A set of experiments was designed by central composite design to process modeling and statistically evaluate the
Khairulazhar Jumbri et al.
PloS one, 10(12), e0144664-e0144664 (2015-12-15)
Kojic acid is widely used to inhibit the browning effect of tyrosinase in cosmetic and food industries. In this work, synthesis of kojic monooleate ester (KMO) was carried out using lipase-catalysed esterification of kojic acid and oleic acid in a
Safa Oufensou et al.
Molecules (Basel, Switzerland), 26(3) (2021-01-31)
Onychomycosis is a common nail infection mainly caused by species belonging to the F. oxysporum, F. solani, and F. fujikuroi species complexes. The aim of this study was to evaluate the in vitro susceptibility of six representative strains of clinically
Chia-Hung Kuo et al.
International journal of molecular sciences, 13(9), 11694-11704 (2012-10-31)
Wax esters are long-chain esters that have been widely applied in premium lubricants, parting agents, antifoaming agents and cosmetics. In this study, the biocatalytic preparation of a specific wax ester, cetyl octanoate, is performed in n-hexane using two commercial immobilized
Eva Puchl'ová et al.
Molecules (Basel, Switzerland), 25(14) (2020-07-18)
The advantageous properties of ethylene glycol diacetate (EGDA) qualify it as a useful substitute for glycerol triacetate (GTA) for various green applications. We scrutinised the lipase-mediated acetylation of structurally diverse alcohols in neat EGDA furnishing the range of naturally occurring
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