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Merck
CN

631396

4-(Aminomethyl)benzonitrile hydrochloride

97%

Synonym(s):

4-Cyanobenzylamine hydrochloride

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About This Item

Linear Formula:
NH2CH2C6H4CN · HCl
CAS Number:
Molecular Weight:
168.62
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

274-279 °C (lit.)

functional group

amine, nitrile

SMILES string

Cl[H].NCc1ccc(cc1)C#N

InChI

1S/C8H8N2.ClH/c9-5-7-1-2-8(6-10)4-3-7;/h1-4H,5,9H2;1H

InChI key

QREZLLYPLRPULF-UHFFFAOYSA-N

Application

4-(Aminomethyl)benzonitrile hydrochloride can be used in the synthesis of fluorescent-labeled bisbenzamidine, which can be a biochemical tool in biomedical studies. It can also be used in the synthesis of 3-(p-benzylamino)-1,2,4,5 tetrazine, used in the modification of alginate hydrogels, employed in cell engineering applications.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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"Versatile click alginate hydrogels crosslinked via tetrazine?norbornene chemistry"
Desai.MR, et al.
Biomaterials, 50, 30-37 (2015)
"Synthesis of a Fluorescent-Labeled Bisbenzamidine Containing the Central (6, 7-Dimethoxy-4-coumaryl) Alanine Building Block"
Haubler D and Gutschow M
Heteroatom Chem., 26(05), 367-337 (2015)
R Voegeli et al.
International journal of cosmetic science, 39(2), 109-120 (2016-07-20)
The aim of this study was to optimize the synthesis of the plasmin and urokinase (uPA) inhibitor benzylsulfonyl-D-Ser-homoPhe-(4-amidino-benzylamide) (BSFAB), to characterize its activity and mechanism of action and to assess its use to improve stratum corneum (SC) barrier function. Peptide



Global Trade Item Number

SKUGTIN
631396-5G04061832101392
631396-25G04061832101385