9-Bromo-1-nonanol - ≥98% , CAS No.55362-80-6

CAS: 55362-80-6 Cat. No.: B124493 Molecular Weight: 223.15 Beilstein Registry Number: 1(2)455 EC Number: 611-262-6

GRADE & PURITY ≥98%

Synonyms

9-Bromo-1-nonanol, 97% | J-650385 | MFCD00063348 | Q-200570 | Amanda (TN) | EN300-6740901 | DTXSID8069016 | AKOS015856511 | BBL103176 | SY015344 | BCP12992 | 9-bromononanol | B1785 | J-650011 | 1-Nonanol, 9-bromo- | C9H19BrO | AMY4021 | STL556986 | 9,9-Bi

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Application

228,229

Specifications

Synonyms

9-Bromo-1-nonanol, 97% | J-650385 | MFCD00063348 | Q-200570 | Amanda (TN) | EN300-6740901 | DTXSID8069016 | AKOS015856511 | BBL103176 | SY015344 | BCP12992 | 9-bromononanol | B1785 | J-650011 | 1-Nonanol, 9-bromo- | C9H19BrO | AMY4021 | STL556986 | 9, 9-Bi

Specifications & Purity

≥98%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488187427
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187427
• Canonical Smiles: C(CCCCO)CCCCBr
• IUPAC Name: 9-bromononan-1-ol
• InChIKey: USJDOLXCPFASNV-UHFFFAOYSA-N
• INCHI: 1S/C9H19BrO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2
• Isomeric SMILES: C(CCCCO)CCCCBr
• WGK Germany: 3
• Molecular Weight: 223.15
• Beilstein: 1(2)455
• Reaxy-Rn: 1737525
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1737525&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: 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
• Description: 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

Chemical and Physical Properties

• Solubility: Soluble in dichloromethane, ethyl acetate and hexane
• Sensitivity: Heat and Air sensitive
• Flash Point(°F): 228.2 °F
• Flash Point(°C): 109 °C
• Boil Point(°C): 125-126°C
• Melt Point(°C): 33-35°C
• Molecular Weight: 223.150 g/mol
• XLogP3: 3.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 222.062 Da
• Monoisotopic Mass: 222.062 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 66.600
• 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

References

1. Weilong Chen, Kun Wu, Bingfei Nan, Mangeng Lu.  (2019)  High thermal conductivity and excellent flexibility of crystalline polyesters with flexible segments in main chains.  REACTIVE & FUNCTIONAL POLYMERS,      [PMID:] [10.1016/j.reactfunctpolym.2019.104370]

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]