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251194

Sigma-Aldrich

1-Fluoropentane

98%

Synonym(s):

Amyl fluoride

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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

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.)

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.

Application

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

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-9.4 °F - closed cup

Flash Point(C)

-23 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

251194-25G:
251194-5G:
251194-VAR:
251194-BULK:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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1-Pentanol ACS reagent, ≥99%

Sigma-Aldrich

398268

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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
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
The role of the solvent in the dual luminescence of 4-N, N-dimethylaminobenzonitrile.
Suppan P.
Chemical Physics Letters, 128(2), 160-161 (1986)

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