(±)-sec-Butylamine - ≥99% , CAS No.13952-84-6

CAS: 13952-84-6 Cat. No.: B105239 Peso molecular: 73.14 Beilstein Registry Number: 1361345 Número EC: 237-732-7

GRADE & PURITY ≥99%

Synonyms

2-Butanamine | 2-AB (VAN) | (-)-sec-Butylamine | C18706 | sec-butylamin | Q288208 | FEMA NO. 4240 | FT-0604436 | sec.butylamine | sec.-butylamine | sec-Butylamine, analytical standard | sec-BUTYLAMINE, HYDROCHLORIDE | Caswell No. 125 | sec butylamine | se

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Specifications

Sinónimos

2-Butanamine | 2-AB (VAN) | (-)-sec-Butylamine | C18706 | sec-butylamin | Q288208 | FEMA NO. 4240 | FT-0604436 | sec.butylamine | sec.-butylamine | sec-Butylamine, analytical standard | sec-BUTYLAMINE, HYDROCHLORIDE | Caswell No. 125 | sec butylamine | se

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

FedEx DG Service

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

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488182931
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182931
• Sonrisas canónicas: CCC(C)N
• IUPAC Name: butan-2-amine
• InChIKey: BHRZNVHARXXAHW-UHFFFAOYSA-N
• INCHI: 1S/C4H11N/c1-3-4(2)5/h4H,3,5H2,1-2H3
• Isómeros SMILES: CCC(C)N
• WGK Alemania: 2
• RTECS: EO3325000
• Número ONU: 2735
• Grupo de embalaje: I
• Peso molecular: 73.14
• Beilstein: 1361345
• Reaxy-Rn: 1361345
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1361345&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Primary amines
          • Level6 Monoalkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Primary amines
• Direct Parent: Monoalkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organopnictogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
• External Descriptors: an amine

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.
• Sensibilidad: air & light & heat sensitive
• Índice de refracción: 1.3928
• Punto de inflamación (°F): -2.2 °F
• Punto de inflamación (°C): -19℃
• Punto de ebullición (°C): 62.5°C
• Punto de fusión (°C): -72°C
• Peso molecular: 73.140 g/mol
• XLogP3: 0.600
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 73.0891 Da
• Monoisotopic Mass: 73.0891 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 19.600
• 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. Bin Liu, Haoliang Ruan, Chengyi Li, Jie Yao, Bei Wei, Lei Wang, Shurong Ban, Jun Xie.  (2023)  Ce-doped indium oxide nanozymes with peroxidase-like activity induced by cerium–indium synergy for colourimetric detection of H2O2.  NEW JOURNAL OF CHEMISTRY,  47  (39): (18476-18484).  [PMID:] [10.1039/D3NJ02985A]

2. Han Xiangning, Lin Hong, Chen Xiangfeng, Wang Luefeng, Zhang Ziang, Wei Xiaojing, Sun Xun, Xie Hanyi, Pavase Tushar Ramesh, Cao Limin, Sui Jianxin.  (2023)  Amide-containing neoepitopes: the key factor in the preparation of hapten-specific antibodies and a strategy to overcome.  Frontiers in Immunology,      [PMID:37342337] [10.3389/fimmu.2023.1144020]

3. Gaokui Chen, Qiuwan Shen, Xin Zhang, Zhongwen Cai, Zicheng Shao, Shian Li, Guogang Yang.  (2023)  Methanol Steam Reforming over La1-xSrxCeO3-δ Catalysts for Hydrogen Production: Optimization of Operating Parameters.  Catalysts,  13  (2): (248).  [PMID:] [10.3390/catal13020248]

4. Yani Zhang, Yue Peng, Chizhong Wang, Kezhi Li, Shuai Liu, Xiansheng Li, Jianjun Chen, Junhua Li.  (2018)  Selective Catalytic Reduction of NOx with Ammonia over Copper Ion Exchanged SAPO-47 Zeolites in a Wide Temperature Range.  ChemCatChem,  10  (11): (2481-2487).  [PMID:] [10.1002/cctc.201800169]

5. Hangzhi Wu, Shuyue Wen, Xiaomin Zhang, Shule Zhang, Xuefeng Guo, Youting Wu.  (2024)  Aqueous solutions of sterically hindered amino acid ionic liquids for rapid and efficient capture of CO2.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.150771]