1-Octanol (n-Octanol) is an ionic liquid and a linear alcohol having an aromatic odor.It has a relatively high boiling point, low water solubility and moderate viscosity. It can be synthesized from capric esters via catalytic hydrogenation. Its oxidative decomposition in the presence of anchored photocatalysts (anchored titanium oxide catalysts and standard TiO2 powder) has been investigated. Its liquid-phase oxidation to 1-octanal in the presence of Ti/Si binary oxide catalysts has been reported. It has gained wide recognition as an extraction solvent in analytical chemistry.

application：

1-Octanol may be used in the preparation of crystalline poly(vinylidene fluoride) (PVDF) membranes.

Specifications

Sinónimos

Especificaciones y pureza

AR, ≥99%

Mecanismos bioquímicos y fisiológicos

阻断 T 型 Ca2+ 通道

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Pureza

≥99%

Nombres e identificadores

Pubchem Sid	508813857
Sonrisas canónicas	CCCCCCCCO
IUPAC Name	octan-1-ol
InChIKey	KBPLFHHGFOOTCA-UHFFFAOYSA-N
INCHI	1S/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H3
Isómeros SMILES	CCCCCCCCO
RTECS	RH6550000
CAS alternativo	220713-26-8,68603-15-6,111-87-5
Número NSC	9823
Términos de entrada MeSH	1 Octanol;1-Octanol;Alcohol, n-Octyl;n Octanol;n Octyl Alcohol;n-Octanol;n-Octyl Alcohol
Peso molecular	130.23
Reaxy-Rn	1697461
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697461&ln=

Documentation

📋 Safety Data Sheet (SDS)

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Clase Fatty Acyls
    - Subclass Fatty alcohols

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Clase	Fatty Acyls
Subclass	Fatty alcohols
Intermediate Tree Nodes	Not available
Direct Parent	Fatty alcohols
Alternative Parents	Primary alcohols Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound
Descripción	This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
External Descriptors	a small molecule
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estructura 3D

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Mecanismos de acción

Certificados (CoA, COO, BSE/TSE y tabla de análisis)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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38 results found

Lot Number	Certificate Type	Fecha	Articulo
H2617137	Certificate of Analysis	Aug 07, 2026	O103325
H2617136	Certificate of Analysis	Aug 07, 2026	O103325
I2628055	Certificate of Analysis	Aug 07, 2026	O103325
I2628054	Certificate of Analysis	Aug 07, 2026	O103325
H2617135	Certificate of Analysis	Aug 07, 2026	O103325
I2628052	Certificate of Analysis	Aug 07, 2026	O103325
I2628053	Certificate of Analysis	Aug 07, 2026	O103325
E2613593	Certificate of Analysis	Apr 30, 2026	O103325
E2613119	Certificate of Analysis	Apr 30, 2026	O103325
E2613120	Certificate of Analysis	Apr 30, 2026	O103325
E2613121	Certificate of Analysis	Apr 30, 2026	O103325
K2525278	Certificate of Analysis	Nov 15, 2025	O103325
K2525277	Certificate of Analysis	Nov 15, 2025	O103325
K2525276	Certificate of Analysis	Nov 15, 2025	O103325
K2525263	Certificate of Analysis	Nov 15, 2025	O103325
I2114295	Certificate of Analysis	Jun 09, 2025	O103325
G2130293	Certificate of Analysis	May 12, 2025	O103325
D2122285	Certificate of Analysis	Feb 07, 2025	O103325
E2429488	Certificate of Analysis	May 16, 2024	O103325
F2528108	Certificate of Analysis	May 16, 2024	O103325
E2429467	Certificate of Analysis	May 16, 2024	O103325
E2429466	Certificate of Analysis	May 16, 2024	O103325
E2429465	Certificate of Analysis	May 16, 2024	O103325
L2420519	Certificate of Analysis	May 16, 2024	O103325
G2415778	Certificate of Analysis	Apr 29, 2024	O103325
A23311287	Certificate of Analysis	Dec 13, 2022	O103325
B2401048	Certificate of Analysis	Dec 13, 2022	O103325
A23311293	Certificate of Analysis	Dec 13, 2022	O103325
A23311292	Certificate of Analysis	Dec 13, 2022	O103325
A2312304	Certificate of Analysis	Dec 13, 2022	O103325
D2122287	Certificate of Analysis	Nov 28, 2022	O103325
D2122286	Certificate of Analysis	Nov 28, 2022	O103325
D2122284	Certificate of Analysis	Nov 28, 2022	O103325
J22181060	Certificate of Analysis	Oct 12, 2022	O103325
J22181073	Certificate of Analysis	Oct 12, 2022	O103325
G2328045	Certificate of Analysis	Jul 19, 2021	O103325
G2304044	Certificate of Analysis	Jul 19, 2021	O103325
J2331078	Certificate of Analysis	Jul 19, 2021	O103325

Propiedades químicas y físicas

Solubilidad	Insoluble in water, soluble in ethanol, ether, and chloroform. Miscellaneous with ethanol, ether and propylene glycol Impossible with water
Sensibilidad	Moisture & heat sensitive.
Índice de refracción	1.4295
Punto de inflamación (°F)	181.4 °F
Punto de inflamación (°C)	83℃
Punto de ebullición (°C)	194.45°C
Punto de fusión (°C)	-16°C(lit.)
Peso molecular	130.229 g/mol
XLogP3	3.000
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	6
Exact Mass	130.136 Da
Monoisotopic Mass	130.136 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	43.800
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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Triphenylphosphine Dibromide (PPh₃Br₂) Is More Than Just a Brominating Reagent: Experimental Selection Logic from Alcohol-to-Alkyl Bromide Conversion to Carboxylic Acid Activation and One-Pot Esterification, Vinyl Bromide Formation, and Nitrile Constructi

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How Alkyl Polyglucosides (APG) Differ from Cocamidopropyl Betaine (CAPB): Structure, Foam Performance, and Applications in Personal Care and Household-Care Formulations

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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APG CAPB

Role of Alkyl Glucosides APG in Cleaning Formulations: Structural Features, Core Performance, and Selection Considerations

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Decyl Glucoside Lauryl Glucoside Coco-Glucoside Caprylyl/Capryl Glucoside

Design Logic of Fluorinated 3,3-Disubstituted Oxetane Building Blocks: Structural Construction and Modulation of Amine Basicity, Lipophilicity, and Metabolic Stability

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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logP logD pKₐ fluorinated oxetane 3,3-disubstituted oxetane molecular building block amine basicity microsomal stability matched molecular pair

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n-Octanol - AR, ≥99% , CAS No.111-87-5

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Descripción general

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n-Octanol - AR, ≥99% , CAS No.111-87-5

Storage & shipping

Quality documents

Literature proof

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Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

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