3-Picolylamine - ≥99%(GC) , CAS No.3731-52-0

CAS: 3731-52-0 Cat. No.: P160053 Peso molecular: 108.14 Beilstein Registry Number: 108056 Número EC: 223-091-0 PubChem CID: 31018

GRADE & PURITY ≥99%(GC)

Synonyms

1-(Pyridin-3-yl)methanamine | AB00752 | NSC 59706 | PICOLAMINE [WHO-DD] | Picolaminum [INN-Latin] | Z104474366 | AC-3071 | Picolamine [INN:DCF] | NCGC00166118-01 | pyridin-3-ylmethyl amine | HMS3264A22 | 3-picolyl amine | Picolamine | 1-Naphthol 2,3,4-Tri

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

1-(Pyridin-3-yl)methanamine | AB00752 | NSC 59706 | PICOLAMINE [WHO-DD] | Picolaminum [INN-Latin] | Z104474366 | AC-3071 | Picolamine [INN:DCF] | NCGC00166118-01 | pyridin-3-ylmethyl amine | HMS3264A22 | 3-picolyl amine | Picolamine | 1-Naphthol 2, 3, 4-Tri

Especificaciones y pureza

≥99%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥99%(GC)

Nombres e identificadores

• Pubchem Sid: 488183123
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183123
• Sonrisas canónicas: C1=CC(=CN=C1)CN
• IUPAC Name: pyridin-3-ylmethanamine
• InChIKey: HDOUGSFASVGDCS-UHFFFAOYSA-N
• INCHI: 1S/C6H8N2/c7-4-6-2-1-3-8-5-6/h1-3,5H,4,7H2
• Isómeros SMILES: C1=CC(=CN=C1)CN
• WGK Alemania: 3
• PubChem CID: 31018
• Número ONU: 2735
• Grupo de embalaje: III
• Peso molecular: 108.14
• Beilstein: 108056
• Reaxy-Rn: 108056

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aralkylamines
• Alternative Parents: Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aralkylamine - Pyridine - Heteroaromatic compound - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
• 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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Fully miscible in water. Soluble in chloroform, ethyl acetate and methanol.
• Sensibilidad: air sensitive
• Índice de refracción: 1.55
• Punto de inflamación (°F): 226.4 °F
• Punto de inflamación (°C): 108 °C
• Punto de ebullición (°C): 73-74°C/1mmHg
• Punto de fusión (°C): -21 °C
• Peso molecular: 108.140 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 108.069 Da
• Monoisotopic Mass: 108.069 Da
• Topological Polar Surface Area: 38.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 63.500
• 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

Referencias

1. Yongfu Zeng, Qian Li, Ruoyu Zhang, Maolin Wei, Xiaochan Zhao, Liping Hao, Haoran Zhang, Ziqing Wang, Xiujuan Guo, Lianfeng Ai.  (2024)  Development and application of a sensitive liquid chromatography-tandem mass spectrometry method for the quantitative analysis of 11 free fatty acids in human serum using a derivatisation strategy.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38810573] [10.1016/j.chroma.2024.465019]

2. Yan Wang, Wanxiang Zhang, Shuhang Ren, Yucui Hou, Weize Wu.  (2024)  Rapid Absorption and Desorption of CO2 by Deep Eutectic Solvents via Reversible CO2-Triggered Proton Transfer Process.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.3c06769]

3. Congfei Zhu, Bingru Wang, Yasen Dai, Yujia Liu, Shuhang Ren, Zhigang Lei, Minjie Gao, Weize Wu.  (2026)  A novel approach to high-pressure CO2 absorption with deep eutectic solvents: Quantitative analysis of physicochemical contribution and low regeneration energy insight.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.174066]