1,2-Epoxy-5-hexene - ≥96%(GC) , CAS No.10353-53-4

CAS: 10353-53-4 Cat. No.: E156386 Formula: C₆H₁₀O Peso molecolare: 98.15 Beilstein Registry Number: 17(5)1,103 Numero EC: 233-771-9

GRADE & PURITY ≥96%(GC)

Synonyms

EINECS 233-771-9 | J-640009 | CCRIS 3748 | SY245295 | 1,2-Epoxy-5-hexene | 2-(but-3-en-1-yl)oxirane | Oxirane, 3-butenyl- | Oxirane, 2-(3-buten-1-yl)- | AKOS015855776 | E0410 | J-640390 | (S)-2-(3-butenyl)oxirane | 1-Hexene, 5,6-epoxy- | BRN 0104509 | F17

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinonimi

EINECS 233-771-9 | J-640009 | CCRIS 3748 | SY245295 | 1,2-Epoxy-5-hexene | 2-(but-3-en-1-yl)oxirane | Oxirane, 3-butenyl- | Oxirane, 2-(3-buten-1-yl)- | AKOS015855776 | E0410 | J-640390 | (S)-2-(3-butenyl)oxirane | 1-Hexene, 5,6-epoxy- | BRN 0104509 | F17

Specifiche e purezza

≥96%(GC)

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

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

Purezza

≥96%(GC)

Nomi e identificatori

• Pubchem Sid: 504754058
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754058
• Sorrisi canonici: C=CCCC1CO1
• IUPAC Name: 2-but-3-enyloxirane
• InChIKey: MUUOUUYKIVSIAR-UHFFFAOYSA-N
• INCHI: 1S/C6H10O/c1-2-3-4-6-5-7-6/h2,6H,1,3-5H2
• Isomeri SMILES: C=CCCC1CO1
• RTECS: MP6780000
• Peso molecolare: 98.15
• Beilstein: 17(5)1,103
• Reaxy-Rn: 104509
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104509&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Epoxides

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Epoxides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Epoxides
• Alternative Parents: Oxacyclic compounds Dialkyl ethers Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oxacycle - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as epoxides. These are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
• 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

• Solubilità: (Soluble) methanol
• Sensibilità: Moisture sensitive
• Indice di rifrazione: 1.425
• Punto di infiammabilità (°F): 60.8 °F
• Punto di infiammabilità (°C): 16 °C
• Punto di ebollizione (°C): 119-121 °C(lit.)
• Peso molecolare: 98.140 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 98.0732 Da
• Monoisotopic Mass: 98.0732 Da
• Topological Polar Surface Area: 12.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 68.600
• 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

Riferimenti

1. Yi Yan, Zifang Peng, Luyan Meng, Wenfen Zhang, Chuan-Fan Ding, Shusheng Zhang.  (2025)  One-step synthesis of high-hydrophilic hydrothermal spheres for N-glycosylated peptides and exosomes analysis in diabetes serum.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:40743645] [10.1016/j.jchromb.2025.124748]