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177490

Sigma-Aldrich

16-Hydroxyhexadecanoic acid

98%

Synonym(s):

16-Hydroxypalmitic acid, Juniperic acid

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About This Item

Linear Formula:
HO(CH2)15CO2H
CAS Number:
506-13-8
Molecular Weight:
272.42
Beilstein:
1783998
EC Number:
208-028-7
MDL number:
MFCD00002750
UNSPSC Code:
12352100
PubChem Substance ID:
24850642
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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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
Jean-Paul Douliez
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
The importance of water to biocatalysis in organic solvents.
M J Alston et al.
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