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Merck

177490

Sigma-Aldrich

16-Hydroxyhexadecanoic acid

98%

Sinónimos:

16-Hydroxypalmitic acid, Juniperic acid

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About This Item

Fórmula lineal:
HO(CH2)15CO2H
Número de CAS:
Peso molecular:
272.42
Beilstein/REAXYS Number:
1783998
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

mp

94-98 °C (lit.)

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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B Grausem et al.
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
Nejumal K Khalid et al.
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
Peiyao Zhu et al.
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.
M J Alston et al.
Biochemical Society transactions, 23(1), 70S-70S (1995-02-01)
Sapa Hima Rani et al.
The Journal of biological chemistry, 285(49), 38337-38347 (2010-10-06)
A key step in the triacylglycerol (TAG) biosynthetic pathway is the final acylation of diacylglycerol (DAG) by DAG acyltransferase. In silico analysis has revealed that the DCR (defective in cuticular ridges) (At5g23940) gene has a typical HX(4)D acyltransferase motif at

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