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74250

Nonane

analytical standard

Synonym(s):

n-Nonane

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About This Item

Linear Formula:
CH3(CH2)7CH3
CAS Number:
111-84-2
Molecular Weight:
128.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329765577
EC Number:
203-913-4
Beilstein/REAXYS Number:
1696917
MDL number:
MFCD00009574
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grade

analytical standard

Quality Level

100

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

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

Application

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

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signalword

Danger

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

3 - Flammable liquids

wgk

WGK 3

flash_point_f

87.8 °F - closed cup

flash_point_c

31.0 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC8731
BCBZ2023
BCBV1972
BCBS3396V
BCBP9705V

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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
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(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
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Global Trade Item Number

SKUGTIN
74250-50ML04061832886404