Pyridine - ≥99% , CAS No.110-86-1

CAS: 110-86-1 Cat. No.: P598447 Fórmula: C₅H₅N Peso molecular: 79.1 Beilstein Registry Number: 103233 Número EC: 203-809-9

GRADE & PURITY ≥99%

Synonyms

PYRIDINE|Azabenzene|110-86-1|Azine|Pyridin|Piridina|Pirydyna|Pyridin [German]|Pirydyna [Polish]|Piridina [Italian]|RCRA waste number U196|Caswell No. 717|NCI-C55301|FEMA No. 2966|FEMA Number 2966|CCRIS 2926|HSDB 118|CHEBI:16227|CP 32|EINECS 203-809-9|NSC

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

FedEx DG Service

Specifications

Sinónimos

PYRIDINE | Azabenzene | 110-86-1 | Azine | Pyridin | Piridina | Pirydyna | Pyridin [German] | Pirydyna [Polish] | Piridina [Italian] | RCRA waste number U196 | Caswell No. 717 | NCI-C55301 | FEMA No. 2966 | FEMA Number 2966 | CCRIS 2926 | HSDB 118 | CHEBI:16227 | CP 32 | EINECS 203-809-9 | NSC

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Protected from light,Room temperature,Argon charged,Desiccated

Enviado en

FedEx DG Service

Pureza

≥99%

Nombres e identificadores

Pubchem Sid

508812912

Sonrisas canónicas

C1=CC=NC=C1

IUPAC Name

pyridine

InChIKey

JUJWROOIHBZHMG-UHFFFAOYSA-N

INCHI

1S/C5H5N/c1-2-4-6-5-3-1/h1-5H

Isómeros SMILES

C1=CC=NC=C1

WGK Alemania

2

RTECS

UR8400000

Número ONU

1282

Grupo de embalaje

II

Peso molecular

79.1

Beilstein

103233

Reaxy-Rn

103233

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=103233&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyridines and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyridines and derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridines and derivatives
• Alternative Parents: Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyridines and derivatives. These are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
• External Descriptors: a ring

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

NAPRT Tchem Nicotinate phosphoribosyltransferase (2 Activities)

Discover Target: NAPRT

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TBXAS1 Tchem Thromboxane-A synthase (3355 Activities)

Discover Target: TBXAS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NAPRT Tchem Nicotinate phosphoribosyltransferase (37 Activities)

Discover Target: NAPRT

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Lithobates pipiens (29 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

E Lysozyme (95 Activities)

Discover Target: E

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

lef Anthrax lethal factor (7585 Activities)

Discover Target: lef

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Chrna3 Neuronal acetylcholine receptor (756 Activities)

Discover Target: Chrna3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in most organic solvents such as water, alcohol and ether.
• Sensibilidad: Light sensitive.moisture sensitive
• Índice de refracción: 1.5092
• Punto de inflamación (°F): 68.0 °F - closed cup
• Punto de inflamación (°C): 20 °C - closed cup
• Punto de ebullición (°C): 115°C
• Punto de fusión (°C): -42°C
• Peso molecular: 79.100 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 79.0422 Da
• Monoisotopic Mass: 79.0422 Da
• Topological Polar Surface Area: 12.900 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 30.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1