2-Piperidineethanol - ≥96%(GC) , CAS No.1484-84-0

CAS: 1484-84-0 Cat. No.: P160104 Peso molecular: 129.2 Beilstein Registry Number: 21(2)85 Número EC: 216-059-2 PubChem CID: 15144

GRADE & PURITY ≥96%(GC)

Synonyms

2-(2-Hydroxyethyl)piperidine | 2-(2-hydroxyethyl)-piperidine | 2-(2-Piperidinyl)ethanol | 2-Ethanolpiperidine, 95per cent | SB42990 | NSC-9261 | EHY6X8X6JQ | (+/-)-2-piperidineethanol | 2-(2-Piperidinyl)ethanol # | EN300-21001 | InChI=1/C7H15NO/c9-6-4-7-3

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

2-(2-Hydroxyethyl)piperidine | 2-(2-hydroxyethyl)-piperidine | 2-(2-Piperidinyl)ethanol | 2-Ethanolpiperidine, 95per cent | SB42990 | NSC-9261 | EHY6X8X6JQ | (+/-)-2-piperidineethanol | 2-(2-Piperidinyl)ethanol # | EN300-21001 | InChI=1/C7H15NO/c9-6-4-7-3

Especificaciones y pureza

≥96%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥96%(GC)

Nombres e identificadores

• Pubchem Sid: 504752639
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752639
• Sonrisas canónicas: C1CCNC(C1)CCO
• IUPAC Name: 2-piperidin-2-ylethanol
• InChIKey: PTHDBHDZSMGHKF-UHFFFAOYSA-N
• INCHI: 1S/C7H15NO/c9-6-4-7-3-1-2-5-8-7/h7-9H,1-6H2
• Isómeros SMILES: C1CCNC(C1)CCO
• PubChem CID: 15144
• Peso molecular: 129.2
• Beilstein: 21(2)85
• Reaxy-Rn: 103471

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Piperidines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Piperidines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Piperidines
• Alternative Parents: 1,3-aminoalcohols Dialkylamines Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Piperidine - 1,3-aminoalcohol - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as piperidines. These are compounds containing a piperidine ring, which is a saturated aliphatic six-member ring with one nitrogen atom and five carbon atoms.
• External Descriptors: Not available

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

Propiedades químicas y físicas

• Solubilidad: Soluble in water, methanol
• Sensibilidad: air sensitive;heat sensitive
• Punto de inflamación (°C): 102°C
• Punto de ebullición (°C): 234°C
• Punto de fusión (°C): 38-40 °C
• Peso molecular: 129.199 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 129.115 Da
• Monoisotopic Mass: 129.115 Da
• Topological Polar Surface Area: 32.299 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 75.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Xiang Jin, Dongxu Xie, Zhenbao Zhang, Aobo Liu, Menglin Wang, Jiabao Dai, Xuan Wang, Huanze Deng, Yijie Liang, Yantao Zhao, Peng Wen, Yanfeng Li.  (2023)  In vitro and in vivo studies on biodegradable Zn porous scaffolds with a drug-loaded coating for the treatment of infected bone defect.  Materials Today Bio,      [PMID:38169782] [10.1016/j.mtbio.2023.100885]