Saltar al contenido
Merck
Todas las fotos(1)

Key Documents

Otros documentos

36685

Supelco

2-Aminopyridine

PESTANAL®, analytical standard

Sinónimos:

2-AP, 2-Pyridinamine, 2-Pyridylamine

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización
Todas las fotos(1)

About This Item

Fórmula empírica (notación de Hill):
C5H6N2
Número de CAS:
504-29-0
Peso molecular:
94.11
Beilstein/REAXYS Number:
105785
EC Number:
207-988-4
MDL number:
MFCD00006312
UNSPSC Code:
41116107
PubChem Substance ID:
329755451

grade

analytical standard

Quality Level

100

product line

PESTANAL®

assay

98-100% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

204-210 °C (lit.)

mp

54-58 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

Nc1ccccn1

InChI

1S/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7)

InChI key

ICSNLGPSRYBMBD-UHFFFAOYSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Categorías relacionadas

General description

2-Aminopyridine can be called as structural motifs, which can be encountered in a variety of useful compounds, that includes fluorescent organic materials and therapeutics. It can undergo condensation with an aromatic aldehyde to give the corresponding schiff′s base.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

CorrosionSkull and crossbones
GHS05,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A

Storage Class

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
BCCH4977
BCCC8118
BCBW1271
BCBT7385
SZBC130XV

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

Busque por un COA

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Pd?PEPPSI?IPentCl: A Useful Catalyst for the Coupling of 2?Aminopyridine Derivatives
Khadra A, et al.
Chemistry?A European Journal, 23, 3206-3212 (2017)
A novel approach towards design, synthesis and evaluation of some Schiff base analogues of 2-aminopyridine and 2-aminobezothiazole against hepatocellular carcinoma
Chacko S and Samanta S
Biomedicine and Pharmacotherapy, 89, 162-176 (2017)
Honggen Wang et al.
Journal of the American Chemical Society, 132(38), 13217-13219 (2010-09-09)
A novel and efficient synthesis of pyrido[1,2-a]benzimidazoles through direct intramolecular aromatic C-H amination of N-aryl-2-aminopyridines has been developed. The reaction, cocatalyzed by Cu(OAc)(2) and Fe(NO(3))(3)·9H(2)O, is carried out in DMF under a dioxygen atmosphere. Diversified pyrido[1,2-a]benzimidazoles containing various substitution patterns
Thomas Zengeya et al.
Angewandte Chemie (International ed. in English), 51(50), 12593-12596 (2012-11-06)
Peptide nucleic acids containing thymidine and 2-aminopyridine (M) nucleobases form stable and sequence-selective triple helices with double-stranded RNA at physiologically relevant conditions. The M-modified PNA showed unique RNA selectivity by having two orders of magnitude higher affinity for the double-stranded
Philipp Ottiger et al.
The Journal of chemical physics, 136(17), 174308-174308 (2012-05-16)
The S(1)/S(2) state exciton splittings of symmetric doubly hydrogen-bonded gas-phase dimers provide spectroscopic benchmarks for the excited-state electronic couplings between UV chromophores. These have important implications for electronic energy transfer in multichromophoric systems ranging from photosynthetic light-harvesting antennae to photosynthetic
Ver todos los artículos relacionados

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico