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Merck

472328

1-Octanol

ACS reagent, ≥99%

Sinónimos:

Alcohol C8, Capryl alcohol, Octyl alcohol

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Fórmula lineal:
CH3(CH2)7OH
Número CAS:
Peso molecular:
130.23
EC Number:
203-917-6
UNSPSC Code:
12352104
PubChem Substance ID:
Beilstein/REAXYS Number:
1697461
MDL number:
NACRES:
NA.21
Assay:
≥99%
Grade:
ACS reagent
Bp:
196 °C (lit.)
Vapor pressure:
0.14 mmHg ( 25 °C)
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grade

ACS reagent

Quality Level

vapor density

4.5 (vs air)

vapor pressure

0.14 mmHg ( 25 °C)

assay

≥99%

form

liquid

autoignition temp.

523 °F

expl. lim.

8 %

dilution

(for analytical testing)

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)

General description

1-Octanol (n-octanol) is a monohydroxy alcohol that can be found in essential oils as the butyrate and acetate. It can be synthesized with high selectivity from biomass-derived furfural-acetone (FFA) in the presence of Pd/NbOPO4 (palladium/ niobium oxide phosphate) catalyst. 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. The performance of molybdenum carbide/zirconium dioxide (Mo2C/ZrO2) catalyst for the hydrodeoxygenation (HDO) of phenol has been analyzed in 1-octanol. 1-Octanol shows promising combustion properties to be employed as a biofuel for spark-ignition engines.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

Application


  • Characterization of Volatile Compounds: This study utilizes 1-Octanol in the analysis of volatile compounds in Valencia orange juice. It highlights its use in the food industry, particularly in quality control and assurance, which is essential for researchers and professionals in the food science sector (Han et al., 2024).

  • Noncontact In Situ Multidiagnostic NMR/Dielectric Spectroscopy: The study discusses the application of 1-Octanol in developing noncontact diagnostic techniques, beneficial for chemists and material scientists involved in analytical and diagnostic methodologies (Morais et al., 2024).

  • Extraction of Bisphenols from Beverages: Highlighting its use in food safety and environmental testing, this study employs 1-Octanol based frameworks for detecting contaminants in consumer products, essential for ensuring public health and safety in the food industry (Cheng et al., 2024).

Biochem/physiol Actions

Bloquea los canales de Ca2+ de tipo T.


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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Clase de almacenamiento

10 - Combustible liquids

flash_point_f

187.7 °F

flash_point_c

86.5 °C



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Eagleson M.
Concise Encyclopedia Chemistry, 744-744 (1994)
Energy-efficient production of 1-octanol from biomass-derived furfural-acetone in water.
Xia Q, et al.
Green Chemistry, 17(8), 4411-4417 (2015)
Tiffany Baiocchi et al.
Genetics, 216(1), 145-157 (2020-07-19)
Chemosensation plays a role in the behaviors and life cycles of numerous organisms, including nematodes. Many guilds of nematodes exist, ranging from the free-living Caenorhabditis elegans to various parasitic species such as entomopathogenic nematodes (EPNs), which are parasites of insects.