Tetramethylene Glycol Monovinyl Ether - ≥99% , CAS No.17832-28-9

CAS: 17832-28-9 Cat. No.: T299067 Molecular Weight: 116.16 Beilstein Registry Number: 1(4)2518 EC Number: 241-793-5

GRADE & PURITY ≥99%

Synonyms

2-(2-(4-(2-methoxyphenyl)piperazin-1-yl)ethyl)-4,4-dimethylisoquinoline-1,3(2H,4H)-dione | Hydroxybutyvinyl ether | EC 241-793-5 | 4-(VINYLOXY)BUTANOL | 4-vinyloxy-1-butanol | 4-ethenoxybutan-1-ol | HBVE | MFCD00080697 | HMBNQNDUEFFFNZ-UHFFFAOYSA-N | 4-(e

Storage

Room temperature

Shipped In

Normal

Overview

Product introduction：

HBVE as monomer in cement additives and as building block in the synthesis of UV-coatings.

Application：

Building block for macro monomers and monomer for vinyl copolymers, reactive diluents for UV coatings. Introduction of side chains with terminated hydroxyl groups into vinyl copolymers. Ethoxylatated HBVE is used as a monomer for concrete additive.

Used for water and solvent based hydroxyfunctional vinyl polymers, which are cross-linked with polyisocyanates and melamine resins.

Specifications

Synonyms

2-(2-(4-(2-methoxyphenyl)piperazin-1-yl)ethyl)-4, 4-dimethylisoquinoline-1, 3(2H, 4H)-dione | Hydroxybutyvinyl ether | EC 241-793-5 | 4-(VINYLOXY)BUTANOL | 4-vinyloxy-1-butanol | 4-ethenoxybutan-1-ol | HBVE | MFCD00080697 | HMBNQNDUEFFFNZ-UHFFFAOYSA-N | 4-(e

Specifications & Purity

≥99%

Legal Information

This product is produced in BASF.

Storage

Room temperature

Shipped In

Normal

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 504755880
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755880
• Canonical Smiles: C=COCCCCO
• IUPAC Name: 4-ethenoxybutan-1-ol
• InChIKey: HMBNQNDUEFFFNZ-UHFFFAOYSA-N
• INCHI: 1S/C6H12O2/c1-2-8-6-4-3-5-7/h2,7H,1,3-6H2
• Isomeric SMILES: C=COCCCCO
• Molecular Weight: 116.16
• Beilstein: 1(4)2518
• Reaxy-Rn: 1700359
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1700359&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: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - 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

• Sensitivity: Light Sensitive
• Refractive Index: 1.444
• Flash Point(°F): 80°C
• Flash Point(°C): 80°C
• Boil Point(°C): 86°C
• Molecular Weight: 116.160 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 116.084 Da
• Monoisotopic Mass: 116.084 Da
• Topological Polar Surface Area: 29.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 52.500
• 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

References

1. Yue Ma, Jinxue Li, Shuhui Li, Zunzhao Li, Wei Zhao, Yuezhen Bin.  (2025)  Intrinsic hydrophobic fluoroethylene-vinyl ester polymer-based superhydrophobic coating with superior anticorrosion properties for metal protection.  Journal of the Taiwan Institute of Chemical Engineers,      [PMID:] [10.1016/j.jtice.2025.106382]