5-Bromo-1-pentanol - technical grade, ≥80%(GC) , CAS No.34626-51-2

CAS: 34626-51-2 Cat. No.: B135090 Peso molecular: 167.05 Beilstein Registry Number: 1(4)1651 Número EC: 628-068-2

GRADE & PURITY Technical grade, ≥80%(GC)

Synonyms

1-Pentanol, 5-bromo- | AKOS009158914 | AS-30544 | SCHEMBL179881 | J-650189 | 5-bromopentanol | 5-bromo-pentanol | BP-31244 | 5-bromopentan-1-ol | MFCD00061101 | FT-0648064 | 1-bromo-5-hydroxypentane | 5-Bromo-1-pentanol, technical, >=80% (GC) | A24616 | 5

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

1-Pentanol, 5-bromo- | AKOS009158914 | AS-30544 | SCHEMBL179881 | J-650189 | 5-bromopentanol | 5-bromo-pentanol | BP-31244 | 5-bromopentan-1-ol | MFCD00061101 | FT-0648064 | 1-bromo-5-hydroxypentane | 5-Bromo-1-pentanol, technical, >=80% (GC) | A24616 | 5

Especificaciones y pureza

technical grade, ≥80%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Grado

Technical grade

Pureza

≥80%(GC)

Nombres e identificadores

• Pubchem Sid: 488187588
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187588
• Sonrisas canónicas: C(CCO)CCBr
• IUPAC Name: 5-bromopentan-1-ol
• InChIKey: WJVQJXVMLRGNGA-UHFFFAOYSA-N
• INCHI: 1S/C5H11BrO/c6-4-2-1-3-5-7/h7H,1-5H2
• Isómeros SMILES: C(CCO)CCBr
• Peso molecular: 167.05
• Beilstein: 1(4)1651
• Reaxy-Rn: 1732316
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1732316&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Not available
• Direct Parent: Primary alcohols
• Alternative Parents: Organobromides Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
• 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

• Sensibilidad: Light Sensitive,Air Sensitive,Heat Sensitive
• Índice de refracción: 1.48
• Punto de inflamación (°C): 40-50°C
• Punto de ebullición (°C): 117 °C/20 mmHg
• Peso molecular: 167.040 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 165.999 Da
• Monoisotopic Mass: 165.999 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 31.300
• 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. Qian Wang, Yong Chen, Yu Liu.  (2013)  Supramolecular ternary polymer mediated by cucurbituril and cyclodextrin.  Polymer Chemistry,  4  (15): (4192-4198).  [PMID:] [10.1039/C3PY00339F]

2. Ze Su, Xiaolong Li, Youye Wang, Long Liu, Yanqiang Zhang, Jianguo Zhang, Zhimin Li.  (2026)  Nitrate ester functionalized ionic liquid as energetic plasticizer for HTPB propellant.  Defence Technology,      [PMID:] [10.1016/j.dt.2026.02.013]