1-Octanol

ACS reagent, ≥99%

Sinônimo(s):

Alcohol C₈, Capryl alcohol, Octyl alcohol

Fórmula linear:

CH₃(CH₂)₇OH

CAS Number:

111-87-5

Peso molecular:

130.23

Beilstein:

1697461

Número CE:

203-917-6

Número MDL:

MFCD00002988

Código UNSPSC:

12352104

ID de substância PubChem:

329757303

grau

ACS reagent

Nível de qualidade

200

densidade de vapor

4.5 (vs air)

pressão de vapor

0.14 mmHg ( 25 °C)

Ensaio

≥99%

Formulário

liquid

temperatura de autoignição

523 °F

Lim. expl.

8 %

dilution

(for analytical testing)

Impurezas

≤0.0002 meq/g Titr. acid

resíduo de evaporação

≤0.004%

cor

APHA: ≤10
clear

índice de refração

n20/D 1.429 (lit.)

p.e.

196 °C (lit.)

pf

−15 °C (lit.)

solubilidade

water: partially soluble 107 g/L at 23 °C

densidade

0.827 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCO

InChI

1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3

chave InChI

KBPLFHHGFOOTCA-UHFFFAOYSA-N

Informações sobre genes

mouse ... Chrna1(11435)

Descrição geral

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]

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.

Aplicação

• 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).

Ações bioquímicas/fisiológicas

Blocks T-type Ca²⁺ channels