3-Methoxy-1-propanol - ≥98% , CAS No.1589-49-7

CAS: 1589-49-7 Cat. No.: M107732 Formule: C₄H₁₀O₂ Poids moléculaire: 90.12 Beilstein Registry Number: 1731204 Numéro CE: 433-230-9

GRADE & PURITY ≥98%

Synonyms

3-Methoxy-1-propanol, >=98.0% (GC) | Bis(4-nitrophenyl) sulphide | FT-0671355 | AKOS005292551 | AM20080231 | METHYL ETHER of PROPYLENE GLYCOL (alpha) | 1,3-propylene glycol monomethyl ether | 1-Methoxy-3-hydroxypropane | 1,3-Propanediol Monomethyl Ether |

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

product description:

3-Methoxy-1-propanol is a primary alcohol. Kinetics of the reactions of 3-methoxy-1-propanol with phenyl isocyanate in the presence of metal catalysts has been reported. Selective synthesis of 3-methoxy-1-propanol from methanol and allyl alcohol with metal oxides and zeolites catalysts in the liquid phase has been studied.

Specifications

Synonymes

3-Methoxy-1-propanol, >=98.0% (GC) | Bis(4-nitrophenyl) sulphide | FT-0671355 | AKOS005292551 | AM20080231 | METHYL ETHER of PROPYLENE GLYCOL (alpha) | 1,3-propylene glycol monomethyl ether | 1-Methoxy-3-hydroxypropane | 1,3-Propanediol Monomethyl Ether |

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

• Pubchem Sid: 488184873
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184873
• Sourires canoniques: COCCCO
• IUPAC Name: 3-methoxypropan-1-ol
• InChIKey: JDFDHBSESGTDAL-UHFFFAOYSA-N
• INCHI: 1S/C4H10O2/c1-6-4-2-3-5/h5H,2-4H2,1H3
• Isomères SMILES: COCCCO
• WGK Allemagne: 1
• RTECS: UB7650000
• Poids moléculaire: 90.12
• Beilstein: 1731204
• Reaxy-Rn: 1731204
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1731204&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: Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyl ether - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Description: 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

Propriétés chimiques et physiques

• Solubilité: Miscible with water, miscible with ethanol, benzene, ether, miscible with acetone, methanol
• Indice de réfraction: 1.413
• Point d'éclair (°F): 100.4 °F
• Point d'éclair (°C): 38 °C
• Point d'ébullition (°C): 150-153 °C
• Poids moléculaire: 90.120 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 90.0681 Da
• Monoisotopic Mass: 90.0681 Da
• Topological Polar Surface Area: 29.500 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 21.500
• 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