Octane

Name: Octane
Brand: ALDRICH
Price: 162.75 USD

electronic grade, ≥99.999% metals basis, ≥99% (CP)

Synonym(s):

n-Octane

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About This Item

Linear Formula:

CH₃(CH₂)₆CH₃

CAS Number:

111-65-9

Molecular Weight:

114.23

Beilstein/REAXYS Number:

1696875

EC Number:

203-892-1

MDL number:

MFCD00009556

UNSPSC Code:

12352100

PubChem Substance ID:

24884258

NACRES:

NA.22

Grade:

electronic grade

Assay:

≥99% (CP)
≥99.999% metals basis

Bp:

125-127 °C (lit.)

Vapor pressure:

11 mmHg ( 20 °C)

Key Documents

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grade

electronic grade

Quality Level

100

vapor density

3.9 (vs air)

vapor pressure

11 mmHg ( 20 °C)

assay

≥99% (CP)
≥99.999% metals basis

form

liquid

autoignition temp.

428 °F

expl. lim.

6.5 %

refractive index

n20/D 1.398 (lit.)

bp

125-127 °C (lit.)

mp

−57 °C (lit.)

density

0.703 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCC

InChI

1S/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H3

InChI key

TVMXDCGIABBOFY-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item	74820	412236	296317
Sigma-Aldrich 657042 Octane	Supelco 74820 Octane	Sigma-Aldrich 412236 Octane	Sigma-Aldrich 296317 Hexadecane
grade electronic grade	grade analytical standard	grade reagent grade	grade anhydrous
Quality Level 100	Quality Level 100	Quality Level 200	Quality Level 100
assay ≥99% (CP), ≥99.999% metals basis	assay ≥99.7% (GC)	assay 98%	assay ≥99%
form liquid	form -	form liquid	form liquid
density 0.703 g/mL at 25 °C (lit.)	density 0.703 g/mL at 25 °C (lit.)	density 0.703 g/mL at 25 °C (lit.)	density 0.773 g/mL at 25 °C (lit.)
vapor pressure 11 mmHg ( 20 °C)	vapor pressure 11 mmHg ( 20 °C)	vapor pressure 11 mmHg ( 20 °C)	vapor pressure 1 mmHg ( 105.3 °C)

pictograms

GHS02,GHS08,GHS07,GHS09

signalword

Danger

hcodes

H225,H304,H315,H336,H410

pcodes

P210 - P233 - P273 - P301 + P310 - P303 + P361 + P353 - P331

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

55.4 °F - closed cup

flash_point_c

13 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Random mutagenesis of the nucleotide-binding domain of NRC1 (NB-LRR Required for Hypersensitive Response-Associated Cell Death-1), a downstream signalling nucleotide-binding, leucine-rich repeat (NB-LRR) protein, identifies gain-of-function mutations in the nucleotide-binding pocket.

Daniela J Sueldo et al.

The New phytologist, 208(1), 210-223 (2015-05-27)

Plant nucleotide-binding, leucine-rich repeat (NB-LRR) proteins confer immunity to pathogens possessing the corresponding avirulence proteins. Activation of NB-LRR proteins is often associated with induction of the hypersensitive response (HR), a form of programmed cell death. NRC1 (NB-LRR Required for HR-Associated

The influence of microbial physiology on biocatalyst activity and efficiency in the terminal hydroxylation of n-octane using Escherichia coli expressing the alkane hydroxylase, CYP153A6.

Oluwafemi A Olaofe et al.

Microbial cell factories, 12, 8-8 (2013-01-29)

Biocatalyst improvement through molecular and recombinant means should be complemented with efficient process design to facilitate process feasibility and improve process economics. This study focused on understanding the bioprocess limitations to identify factors that impact the expression of the terminal

Screening method for 11-nor-delta9-tetrahydrocannabinol-9-carboxylic acid in urine using hollow fiber membrane solvent microextraction with in-tube derivatization.

K E Kramer et al.

Journal of chromatography. B, Biomedical sciences and applications, 760(1), 27-36 (2001-08-28)

An efficient and inexpensive screening technique for the simultaneous clean-up, extraction, and derivatization of 11-nor-delta9-tetrahydrocannabinol-9-carboxylic acid (THC-COOH) from urine has been developed. Using the principles of solvent microextraction in the form of a 20-microl volume of solvent placed inside a

Total synthesis of kopsinine.

Jian Xie et al.

Organic letters, 15(4), 868-870 (2013-02-09)

The use of a powerful intramolecular [4 + 2]/[3 + 2] cycloaddition cascade of an 1,3,4-oxadiazole in the divergent total synthesis of kopsinine (1), featuring an additional unique SmI(2)-promoted transannular cyclization reaction for formation of the bicyclo[2.2.2]octane central to its

Direct Methylation of Amines with Carbon Dioxide and Molecular Hydrogen using Supported Gold Catalysts.

Xian-Long Du et al.

ChemSusChem, 8(20), 3489-3496 (2015-09-15)

The N-methylation of amines with CO2 and H2 is an important step in the synthesis of bioactive compounds and chemical intermediates. The first heterogeneous Au catalyst is reported for this methylation reaction with good to excellent yields. The average turnover

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