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251194

Sigma-Aldrich

1-Fluoropentane

98%

Synonym(s):

Amyl fluoride

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5 G
$174.00

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5 G
$174.00

About This Item

Linear Formula:
CH3(CH2)4F
CAS Number:
592-50-7
Molecular Weight:
90.14
EC Number:
209-761-5
MDL number:
MFCD00000453
UNSPSC Code:
12352100
PubChem Substance ID:
24855116
NACRES:
NA.22

$174.00

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Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.36 (lit.)

bp

62-63 °C (lit.)

density

0.789 g/mL at 25 °C (lit.)

functional group

alkyl halide
fluoro

SMILES string

CCCCCF

InChI

1S/C5H11F/c1-2-3-4-5-6/h2-5H2,1H3

InChI key

OEPRBXUJOQLYID-UHFFFAOYSA-N

General description

Dual luminescence of 4-N,N-dimethylaminobenzonitrile has been observed in 1-fluoropentane[1].

Application

1-Fluoropentane has been used in the synthesis of 6-F-B10H13 and 6-Cl- B10H13 (halodecaboranes)[2].

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Product No.
Description
Pricing

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-9.4 °F - closed cup

flash_point_c

-23 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV5295
MKCT4715
MKCM5819
MKCL0981
MKCH6617

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Sigma-Aldrich

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1-Pentanol ACS reagent, ≥99%

Sigma-Aldrich

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The role of the solvent in the dual luminescence of 4-N, N-dimethylaminobenzonitrile.
Suppan P.
Chemical Physics Letters, 128(2), 160-161 (1986)
C F Nhachi et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(8), 705-713 (1988-08-01)
Phenobarbitone pretreatment potentiated hepatocyte lesions in male rats 24 hr after treatment with 1-fluoropentane (3.5 mg/kg body weight) and 1-fluorohexane (0.17 mg/kg body weight). Serum levels of the enzymes ornithine carbamyltransferase, glutamic-pyruvic transaminase and gamma-glutamyltranspeptidase were significantly elevated by the
William C Ewing et al.
Inorganic chemistry, 47(19), 8580-8582 (2008-08-30)
The high-yield syntheses of 6-X-B 10H 13 [X = Cl (88%), Br (96%), I (84%)] resulted from the cage-opening reactions of the (NH 4 (+)) 2B 10H 10 (2-) salt with ionic-liquid-based superacidic hydrogen halides, while both the previously unknown
K R Harikumar et al.
Nature chemistry, 1(9), 716-721 (2010-12-03)
The controlled imprinting of surfaces with specified patterns is important in the development of nanoscale devices. Previously, such patterns were created using self-assembled physisorbed adsorbate molecules that can be stabilized on the surface by subsequent chemical bonding. Here we show

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