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Safety Information

23-0130

Sigma-Aldrich

1-Octanol

SAJ first grade, ≥75.0%

Synonym(s):

Alcohol C8, Capryl alcohol, Octyl alcohol

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About This Item

Linear Formula:
CH3(CH2)7OH
CAS Number:
111-87-5
Molecular Weight:
130.23
Beilstein:
1697461
MDL number:
MFCD00002988
UNSPSC Code:
12352104
PubChem Substance ID:
329752363
grade:
SAJ first grade
Assay:
≥75.0%
technique(s):
HPLC: suitable
bp:
196 °C (lit.)
vapor pressure:
0.14 mmHg ( 25 °C)

grade

SAJ first grade

vapor density

4.5 (vs air)

vapor pressure

0.14 mmHg ( 25 °C)

Assay

≥75.0%

form

liquid

autoignition temp.

523 °F

expl. lim.

8 % (lit.)

availability

available only in Japan

technique(s)

HPLC: suitable

refractive index

n20/D 1.429 (lit.)

bp

196 °C (lit.)

mp

−15 °C (lit.)

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

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Related Categories

Biochem/physiol Actions

Blocks T-type Ca2+ channels

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319,H412

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

177.8 °F

Flash Point(C)

81 °C

Regulatory Information

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Lot/Batch Number
A9445
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A2296
A0264
A9247

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Cristian Gobbo et al.
ACS nano, 6(12), 10684-10698 (2012-12-12)
Controlling the molecular conformation of oligomers on surfaces through noncovalent interactions symbolizes an important approach in the bottom-up patterning of surfaces with nanoscale precision. Here we report on the design, synthesis, and scanning tunneling microscopy (STM) investigation of linear oligoamides
B D Anderson et al.
The Journal of investigative dermatology, 93(2), 280-286 (1989-08-01)
The permeability coefficients (kp) of a series of methyl-substituted p-cresols were determined in human stratum corneum along with their partition coefficients (PC) between water and untreated stratum corneum, delipidized stratum corneum, octanol, and heptane. The PC values were identical in
D Southwell et al.
The Journal of investigative dermatology, 80(6), 507-514 (1983-06-01)
Penetration-enhancing solvents may modify diffusional routes through the stratum corneum and the partitioning of drugs into these pathways. To investigate the mechanisms of action of enhancers, steady-state fluxes were measured in vitro for polar methanol, nonpolar octanol, and an intermediate
John A Arnott et al.
Expert opinion on drug discovery, 7(10), 863-875 (2012-09-21)
The role of lipophilicity in drug discovery and design is a critical one. Lipophilicity is a key physicochemical property that plays a crucial role in determining ADMET (absorption, distribution, metabolism, excretion, and toxicity) properties and the overall suitability of drug
Sophie Martel et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(1-2), 21-29 (2012-11-08)
Lipophilicity is a crucial parameter in drug development since it impacts both ADME properties and target affinity of drug candidates. In early drug discovery stage, accurate tools for logP prediction are highly desired. Many calculation methods were developed to aid
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