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162493

Sigma-Aldrich

4-Fluorobenzylamine

97%

Synonym(s):

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

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About This Item

Linear Formula:
FC6H4CH2NH2
CAS Number:
140-75-0
Molecular Weight:
125.14
Beilstein:
636501
EC Number:
205-430-4
MDL number:
MFCD00008120
UNSPSC Code:
12352100
eCl@ss:
39040409
PubChem Substance ID:
24849984
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

refractive index

n20/D 1.512 (lit.)

bp

183 °C (lit.)

density

1.095 g/mL at 25 °C (lit.)

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)

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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
GHS05

Signal Word

Danger

Hazard Statements

H290,H314

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8381
STBF8517V
STBF4450V
STBF3724V
STBC4917V

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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
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