177490
16-Hydroxyhexadecanoic acid
98%
Sinónimos:
16-Hydroxypalmitic acid, Juniperic acid
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About This Item
Productos recomendados
Quality Level
assay
98%
form
solid
mp
94-98 °C (lit.)
functional group
carboxylic acid
hydroxyl
SMILES string
OCCCCCCCCCCCCCCCC(O)=O
InChI
1S/C16H32O3/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h17H,1-15H2,(H,18,19)
InChI key
UGAGPNKCDRTDHP-UHFFFAOYSA-N
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Application
16-Hydroxyhexadecanoic acid was used in the synthesis of dihydroxypalmitic acids. It was also used to induce the expression of two GRP genes of Arabidopsis thaliana, AtGRP5 and AtGRP23.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Los clientes también vieron
Plant, cell & environment, 37(9), 2102-2115 (2014-02-14)
Cutin and suberin represent lipophilic polymers forming plant/environment interfaces in leaves and roots. Despite recent progress in Arabidopsis, there is still a lack on information concerning cutin and suberin synthesis, especially in crops. Based on sequence homology, we isolated two
Environmental monitoring and assessment, 190(6), 370-370 (2018-06-02)
The presence of emerging contaminants (ECs) in different aquatic systems may contribute to hazardous effects on aquatic organisms and subsequently on human health. In the present work, liquid chromatography coupled to a quadrupole time of flight mass spectrometer (LC-Q-ToF-MS) was
Journal of cell communication and signaling, 14(2), 175-192 (2020-01-12)
Esophageal squamous cell carcinoma (ESCC) is one of the most common malignant tumors with poor prognosis. Aryl hydrocarbon receptor (AHR) is a ligand-dependent transcription factor and emerging evidence shows it is associated with tumor initiation and promotion. However, the relationship
The importance of water to biocatalysis in organic solvents.
Biochemical Society transactions, 23(1), 70S-70S (1995-02-01)
Journal of colloid and interface science, 271(2), 507-510 (2004-02-20)
The interaction between cutin and suberin monomers, i.e., omega -hydroxylpalmitic acid, alpha, omega -hexadecanedioic acid, alpha, omega --hexadecanediol, 12-hydroxylstearic acid, and phospholipid vesicles biomimicking the lipid structure of plant cell membranes has been studied by optical and transmission electron microscopy
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