10930
Arachidic acid
synthetic, ≥99.0% (GC)
Sinónimos:
Arachic acid, Arachidinic acid, Eicosanoic acid, Icosanoic acid, NSC 93983
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Fórmula lineal:
CH3(CH2)18COOH
Número CAS:
Peso molecular:
312.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-031-3
Beilstein/REAXYS Number:
1788211
MDL number:
Servicio técnico
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Permítanos ayudarleQuality Level
assay
≥99.0% (GC)
form
solid
quality
synthetic
mp
74-76 °C (lit.)
solubility
H2O: insoluble, benzene: freely soluble, chloroform: freely soluble, cold water: very slightly soluble, diethyl ether: freely soluble, petroleum ether: freely soluble
functional group
carboxylic acid
SMILES string
CCCCCCCCCCCCCCCCCCCC(O)=O
InChI
1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22/h2-19H2,1H3,(H,21,22)
InChI key
VKOBVWXKNCXXDE-UHFFFAOYSA-N
Application
Arachidic acid was used to study the growth of cadmium sulfide crystals under arachidic acid monolayers. It may be used to compose Langmuir-Blodgett (LB) films.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Clase de almacenamiento
11 - Combustible Solids
wgk
nwg
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Epitaxial growth of size-quantized cadmium sulfide crystals under arachidic acid monolayers.
Yang J, et al.
The Journal of Physical Chemistry, 99(15), 5500-5504 (1995)
Morphology of microphase separation in arachidic acid/cadmium arachidate Langmuir-Blodgett multilayers.
Kurnaz ML and Schwartz DK.
The Journal of Physical Chemistry, 100(26), 11113-11119 (1996)
Gillian Groeger et al.
Journal of neurochemistry, 109(5), 1544-1554 (2009-04-07)
Reactive oxygen species (ROS) have traditionally been viewed as a toxic group of molecules; however, recent publications have shown that these molecules, including H(2)O(2), can also strongly promote cell survival. Even though the retina has a large capacity to produce