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Supelco

Nonane

analytical standard

Synonym(s):

n-Nonane

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About This Item

Linear Formula:
CH3(CH2)7CH3
CAS Number:
Molecular Weight:
128.26
Beilstein:
1696917
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

4.41 (vs air)

vapor pressure

0.18 psi ( 37.7 °C)

Assay

≥99.8% (GC)

autoignition temp.

401 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

2.9 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.405 (lit.)
n20/D 1.405

bp

151 °C (lit.)

mp

−53 °C (lit.)

density

0.718 g/mL at 25 °C (lit.)

application(s)

petroleum

format

neat

SMILES string

CCCCCCCCC

InChI

1S/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H3

InChI key

BKIMMITUMNQMOS-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Lip Kim Lee et al.
Applied and environmental microbiology, 76(3), 794-802 (2009-12-17)
Polybrominated diphenyl ethers (PBDEs) have attracted attention recently due to their proven adverse effects on animals and their increasing concentrations in various environmental media and biota. To gain insight into the fate of PBDEs, microcosms established with soils and sediments
Franck Slowinski et al.
Organic letters, 12(21), 5004-5007 (2010-10-14)
New azabicyclo[2.2.1]heptane and -[3.3.1]nonane derivatives containing a pyridinyl substituent at the bridgehead position have been synthesized via an efficient ten chemical steps pathway. Both chemical series were then evaluated in vitro for their affinity at α7 nicotinic receptors revealing nanomolar
Arif Baran et al.
The Journal of organic chemistry, 77(3), 1244-1250 (2012-01-11)
1,3,3a,7a-Tetrahydro-2-benzofuran was used as key compound for the synthesis of various bishomoinositol derivatives. The diene was subjected to an epoxidation reaction for further functionalization of the diene unit. The bisepoxide obtained was submitted to a ring-opening reaction with acid in
Arif Baran et al.
The Journal of organic chemistry, 77(11), 5086-5097 (2012-05-23)
Transformation of cyclohexa-2,4-diene-1,2-diylbis(methylene) diacetate to various carbasugars is described. Photooxygenation of a cyclohexadiene derivative gave a bicyclicendoperoxide, which was reduced with thiourea to [2-[(acetyloxy)methyl]cyclohexa-2,4-dien-1-yl]methyl acetate. Epoxidation of the remaining double bond followed by epoxide ring-opening and hydrolysis of the acetate
Adrian A Accurso et al.
The Journal of organic chemistry, 76(11), 4392-4395 (2011-05-07)
Sulfur-, selenium-, and nitrogen-containing compounds bearing leaving groups in the β-position undergo facile substitution chemistry enabled by anchimeric assistance. Here we provide direct comparisons between such systems in the rigid bicyclo[3.3.1]nonane framework easily derived from 1,5-cyclooctadiene. For a series of

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