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401633

Sigma-Aldrich

1-Pyrenemethylamine hydrochloride

95%

Sinónimos:

PMA

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1 G
MXP 1,677.00
5 G
MXP 6,088.00

MXP 1,677.00

Fecha estimada de envío27 de marzo de 2025

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1 G
MXP 1,677.00
5 G
MXP 6,088.00

About This Item

Fórmula empírica (notación de Hill):
C17H13N · HCl
Número de CAS:
93324-65-3
Peso molecular:
267.75
MDL number:
MFCD00192425
UNSPSC Code:
12352100
PubChem Substance ID:
24865033
NACRES:
NA.22
form:
powder
assay:
95%

MXP 1,677.00

Fecha estimada de envío27 de marzo de 2025

Solicitar un pedido a granel

Quality Level

200

assay

95%

form

powder

mp

258 °C (dec.) (lit.)

functional group

amine

SMILES string

Cl[H].NCc1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C17H13N.ClH/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12;/h1-9H,10,18H2;1H

InChI key

RGNMXKKNDSHTFD-UHFFFAOYSA-N

Categorías relacionadas

General description

1-Pyrenemethylamine hydrochloride is an organic building block.

Application

1-Pyrenemethylamine (PyNH2) has also been used for the synthesis of:
  • Pyrenyl hyaluronan (Py-HA), a pyrenyl-based polymer that can be used for the development of pH-triggered drug carriers.[1]
  • An electrochemical electrode of reduced graphene oxide bound with pyrene functionalized folic acid derivative.[2]

It can also be used for the synthesis of 4,6-dichloro-2-pyrenemethylamine-1,3,5-triazine, a precursor to synthesize a star shaped polymer 4,6-bis(9H-carbazol-2-yloxy)-2-(pyrenemethylamine)-1,3,5 triazine (TPC).[3]
1-Pyrenemethylamine hydrochloride (PyNH2) has been used for the loading of human telomerase reverse transcriptase (hTERT) small interfering RNA (siRNA) to the functionalized graphene oxide (GO) for the tumor targeting delivery of siRNA.[4]
1-Pyrenemethylamine hydrochloride has been used in the preparation of 1-pyrenemethylamine.[5] It may be used for the noncovalent functionalization of SWNTs with cationic moieties which binds strongly to the negatively charged phosphate backbone of the DNA.[6] It may be used in the preparation of the following Schiff-base ligand:
  • pyren-1-ylmethyl-[2-(6-{2-[(pyren-1-ylmethylimino)-methyl]-phenoxymethyl}-pyridin-2-ylmethoxy)-benzylidene]-amine[7]
  • 2(pyren-1-ylmethyl-{2-[6-(2-{[(pyren-1-ylmethyl)-amino]-methyl}- phenoxymethyl)-pyridin-2-ylmethoxy])-benzyl}-amine[7]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCS3461
MKCR1534
MKCQ5955
MKCP5650
MKCP0851

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Reactively formed block and graft copolymers as compatibilizers for polyamide 66/PS blends.
Jeon HK, et al.
Polymer, 45(1), 197-206 (2004)
Fabien Giroud et al.
Biosensors & bioelectronics, 87, 957-963 (2016-09-26)
We report the functionalization of multi-walled carbon nanotubes (MWCNTs) electrodes by a bifunctional nitroaromatic molecule accomplished via π-π interactions of a pyrene derivative. DTNB (5,5'-dithiobis(2-nitrobenzoic acid)) has the particularity to possess both electroactivable nitro groups and negatively charged carboxylic groups.
Sudarat Yenjai et al.
Journal of photochemistry and photobiology. B, Biology, 173, 35-42 (2017-05-30)
A new photochemical reagent, succinic acid-1(1-pyrene)methylamide (PMA-SUC), was developed to recognize the specific binding sites on model proteins, egg-white lysozyme and avidin. The interaction of the photochemical reagent with the proteins was studied by UV-Vis, fluorescence spectroscopic methods and docking
Liwei Hui et al.
ACS nano, 14(10), 13047-13055 (2020-10-14)
We demonstrate area-selective atomic layer deposition (ALD) of oxides on DNA nanostructures. Area-selective ALD of Al2O3, TiO2, and HfO2 was successfully achieved on both 2D and 3D DNA nanostructures deposited on a polystyrene (PS) substrate. The resulting DNA-inorganic hybrid structure
Assembly of chemically reduced graphene oxide with folic acid functionalized with pyrene moieties and electrochemical sensing of folate receptors.
Kwon B, et al.
Carbon Letters, 27(2), 26-34 (2018)
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