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Safety Information

552313

Sigma-Aldrich

4-Phenylbenzylamine

97%

Synonym(s):

(4-Phenylphenyl)methanamine, 1-(Biphenyl-4-yl)methanamine, 4-(Aminomethyl)biphenyl, 4-Biphenylmethylamine, Biphenyl-4-ylmethanamine, [(1,1′-Biphenyl-4-yl)methyl]amine, [(Biphenyl-4-yl)methyl]amine, [1,1′-Biphenyl]-4-ylmethanamine, p-Phenylbenzylamine

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About This Item

Linear Formula:
C6H5C6H4CH2NH2
CAS Number:
Molecular Weight:
183.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

mp

48-53 °C (lit.)

functional group

amine
phenyl

SMILES string

NCc1ccc(cc1)-c2ccccc2

InChI

1S/C13H13N/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9H,10,14H2

InChI key

RMSPOVPGDBDYKH-UHFFFAOYSA-N

Related Categories

Application

4-Phenylbenzylamine may be used in the synthesis of:
  • squaric acid asymmetric diamides of glycopeptide antibiotics
  • asymmetric diamides of daunomycin and carminomycin
  • N-(biphenyl-4-ylmethyl)-1-hydroxy-6-thioxo-1,6-dihydropyridine-2-carboxamide

4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.

Other Notes

Handle and store under nitrogen to limit formation of impurities.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

224.6 °F - closed cup

Flash Point(C)

107 °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.

JAN Code

552313-1G:
552313-VAR:
552313-BULK:
552313-5G:


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A new class of semisynthetic anthracycline glycoside antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 58(11), 704-704 (2005)
A new series of glycopeptide antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 59(9), 564-564 (2006)
chemical society(Great Britain)
Journal of the Chemical Society, Part 1 (1993)
Coupling fast water exchange to slow molecular tumbling in Gd3+ chelates: why faster is not always better.
Avedano S, et al.
Inorganic Chemistry, 52(15), 8436-8450 (2013)
Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor.
Agrawal A, et al.
Journal of Medicinal Chemistry, 52(4), 1063-1074 (2009)

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