Skip to Content
Merck
All Photos(1)

Key Documents

162493

Sigma-Aldrich

4-Fluorobenzylamine

97%

Synonym(s):

(4-Fluorophenyl)methanamine, 1-(4-Fluorophenyl)methanamine, 4-Fluorobenzenemethanamine, [(4-Fluorophenyl)methyl]amine, p-Fluorobenzylamine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
FC6H4CH2NH2
CAS Number:
Molecular Weight:
125.14
Beilstein:
636501
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39040409
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.512 (lit.)

bp

183 °C (lit.)

density

1.095 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCc1ccc(F)cc1

InChI

1S/C7H8FN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2

InChI key

IIFVWLUQBAIPMJ-UHFFFAOYSA-N

Gene Information

human ... AOC3(8639)
mouse ... Aoc3(11754)

Looking for similar products? Visit Product Comparison Guide

General description

[18F]4-fluorobenzylamine reacts with the α- and γ-carboxyl groups of folic acid to yield 18F-labeled folate. It is an important building block for the synthesis of 18F-labeled compounds.

Application

4-Fluorobenzylamine was used in the synthesis of new tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

150.8 °F - closed cup

Flash Point(C)

66 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

3'-Aza-2'-[18F]fluorofolic acid.
Leung K
SourceMolecular Imaging and Contrast Agent Database (MICAD) [Internet] (2013)
Muhammad Kaleem Khosa et al.
Pakistan journal of pharmaceutical sciences, 28(6), 2167-2171 (2015-12-08)
New series of benzophenone imines with general formula Ph2-C=NR; R = Benzyl, 4-Fluorobenzyl, Naphthyl, Phenyl, 4-Nitrophenyl were synthesized by condensation of dichlorodiphenylmethane and different aromatic primary amines (1:1) Those imines were characterized by different physiochemical and spectroscopic techniques like melting
Walkiria Schlindwein et al.
Dalton transactions (Cambridge, England : 2003), (10)(10), 1313-1321 (2006-03-01)
New tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands derived from maltol (3-hydroxy-2-methyl-4-pyrone) or ethylmaltol (2-ethyl-3-hydroxy-4-pyrone), including a variety of N-aryl (phenyl, 4'-tolyl, 4'-(n-butyl)phenyl, 4'-(n-hexyl)phenyl) and N-benzyl (4'-methylbenzyl, 4'-fluorobenzyl and 4'-(trifluoromethyl)benzylamine) substituents on the nitrogen atom of the pyridinone ring, have been prepared.
T Haradahira et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 49(12), 1551-1556 (1998-09-24)
A fluorine-18 labeled analog of an antitumor prostaglandin delta 7-PGA1 methyl ester, 15-deoxy-13,14-dihydro-delta 7-PGA1 4-[18F]fluorobenzyl amide ([18F]3), was synthesized as a tracer candidate for detecting tumors with positron emission tomography. p-[18F]Fluorobenzylamine (p-[18F]FBnA) used as a labeled precursor for the synthesis
Ingrid Koslowsky et al.
Organic & biomolecular chemistry, 8(20), 4730-4735 (2010-08-27)
A novel synthesis of 4-[(18)F]fluorobenzylamine ([(18)F]FBA) by means of transition metal-assisted sodium borohydride reduction of 4-[(18)F]fluorobenzonitrile ([(18)F]FBN) is described. This approach could successfully be extended to borohydride exchange resin (BER) enabling a viable option for use in automated syntheses. [(18)F]FBA

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service