3-Butoxypropylamine - ≥98% , CAS No.16499-88-0

CAS: 16499-88-0 Cat. No.: B152034 Fórmula: C₇H₁₇NO Peso molecular: 131.22 Número CE: 240-566-8

GRADE & PURITY ≥98%

Synonyms

1-Propanamine, 3-butoxy- | J-640304 | AS-31124 | J-800308 | 3-n-Butoxypropylamine | 3-Butoxypropanamine | N-Acetyl-b-D-galactosamine | (s)-3-amino-azepan-2-one | AKOS005292566 | SCHEMBL237526 | ANTIMYCINA | 3-(n-butyloxy)-1-propylamine | 3-butoxypropan-1-

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

1-Propanamine, 3-butoxy- | J-640304 | AS-31124 | J-800308 | 3-n-Butoxypropylamine | 3-Butoxypropanamine | N-Acetyl-b-D-galactosamine | (s)-3-amino-azepan-2-one | AKOS005292566 | SCHEMBL237526 | ANTIMYCINA | 3-(n-butyloxy)-1-propylamine | 3-butoxypropan-1-

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 504755813
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755813
• Sorrisos canónicos: CCCCOCCCN
• IUPAC Name: 3-butoxypropan-1-amine
• InChIKey: LPUBRQWGZPPVBS-UHFFFAOYSA-N
• INCHI: 1S/C7H17NO/c1-2-3-6-9-7-4-5-8/h2-8H2,1H3
• SMILES isoméricas: CCCCOCCCN
• WGK Alemanha: 3
• Peso molecular: 131.22
• Reaxy-Rn: 1734198
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1734198&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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

Propriedades químicas e físicas

• Sensibilidade: air sensitive
• Índice de refração: 1.4250-1.4270
• Ponto de inflamação (°F): 145.4 °F
• Ponto de inflamação (°C): 63°C
• Ponto de ebulição (°C): 169-170 °C
• Peso molecular: 131.220 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 131.131 Da
• Monoisotopic Mass: 131.131 Da
• Topological Polar Surface Area: 35.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 48.200
• 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

Referências

1. Si Yejia, Sun Zhuo, Zhao Qian, Xie Tao, Wu Jingjun.  (2025)  3D printing of salt-like granular polyacrylamide as sacrificial molds for shaping versatile materials.  Nature Communications,  16  (1): (1-10).  [PMID:40764489] [10.1038/s41467-025-62674-1]

2. Wenzi Liang, Chang-An Xu, Limin Man.  (2025)  Lignin grafted pyridinized graphene oxide based self-healing anti-corrosion composite coating.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.138146]