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

CAS: 34626-51-2 Cat. No.: B135090 Formula: C₅H₁₁BrO Peso molecolare: 167.05 Beilstein Registry Number: 1(4)1651 Numero 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

Sinonimi

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

Specifiche e purezza

technical grade, ≥80%(GC)

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Grado tecnico

Purezza

≥80%(GC)

Nomi e identificatori

• Pubchem Sid: 488187588
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187588
• Sorrisi canonici: 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
• Isomeri SMILES: C(CCO)CCBr
• Peso molecolare: 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
    • Classe Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Light Sensitive,Air Sensitive,Heat Sensitive
• Indice di rifrazione: 1.48
• Punto di infiammabilità (°C): 40-50°C
• Punto di ebollizione (°C): 117 °C/20 mmHg
• Peso molecolare: 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

Riferimenti

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]