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Sigma-Aldrich 472328 1-Octanol ACS reagent, ≥99% 1 L
Brand
Stock Code
LB.SA.472328-1L
Kısa Bilgi
Synonym(s): Alcohol C8, Capryl alcohol, Octyl alcohol Linear Formula: CH3(CH2)7OH CAS Number: 111-87-5 Molecular Weight: 130.23 Beilstein: 1697461 EC Number: 203-917-6 MDL number: MFCD00002988 PubChem Substance ID: 329757303
| Sigma-Aldrich 472328 1-Octanol ACS reagent, ≥99% 1 L |
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Synonym(s): Alcohol C8, Capryl alcohol, Octyl alcohol
Linear Formula: CH3(CH2)7OH
CAS Number: 111-87-5
Molecular Weight: 130.23
Beilstein: 1697461
EC Number: 203-917-6
MDL number: MFCD00002988
PubChem Substance ID: 329757303
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PROPERTIES
grade ACS reagent
Quality Level 200
vapor density 4.5 (vs air)
vapor pressure 0.14 mmHg ( 25 °C)
assay ≥99%
form liquid
autoignition temp. 523 °F
expl. lim. 8 %
impurities ≤0.0002 meq/g Titr. acid
evapn. residue ≤0.004%
color APHA: ≤10, clear
refractive index n20/D 1.429 (lit.)
bp 196 °C (lit.)
mp −15 °C (lit.)
solubility water: partially soluble 107 g/L at 23 °C
density 0.827 g/mL at 25 °C (lit.)
SMILES string CCCCCCCCO
InChI 1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3
InChI key KBPLFHHGFOOTCA-UHFFFAOYSA-N
Gene Information mouse ... Chrna1(11435)
DESCRIPTION
General description
1-Octanol (n-octanol) is a monohydroxy alcohol that can be found in essential oils as the butyrate and acetate.[1] It can be synthesized with high selectivity from biomass-derived furfural-acetone (FFA) in the presence of Pd/NbOPO4 (palladium/ niobium oxide phosphate) catalyst.[2] Formation of octyl ether and octyl ester compounds from Chinese fir sawdust by liquefaction in the presence of acidic ionic liquids (AILs) has been reported.[3] The performance of molybdenum carbide/zirconium dioxide (Mo2C/ZrO2) catalyst for the hydrodeoxygenation (HDO) of phenol has been analyzed in 1-octanol.[4] 1-Octanol shows promising combustion properties to be employed as a biofuel for spark-ignition engines.[5]
Packaging
100 mL in glass bottle
1, 2.5, 4 L in glass bottle
Biochem/physiol Actions
Blocks T-type Ca2+ channels |
