4-Vinyloxybutanol

Product Information

Molecular Formula:
C6H12O2
Molecular Weight:
116.16
Description
4-Vinyloxybutanol is a bioactive compound utilized in the biomedical industry. With its unique properties, it has shown potential in the development of drugs targeting various diseases, including cancer and cardiovascular disorders. Extensive studies have been conducted to explore the therapeutic applications and mechanisms of action of 4-Vinyloxybutanol in these fields.
Synonyms
4-Vinyloxybutanol (stabilized with KOH)
IUPAC Name
4-ethenoxybutan-1-ol
Canonical SMILES
C=COCCCCO
InChI
InChI=1S/C6H12O2/c1-2-8-6-4-3-5-7/h2,7H,1,3-6H2
InChI Key
HMBNQNDUEFFFNZ-UHFFFAOYSA-N
Boiling Point
86 °C/13 mmHg
Flash Point
80 °C
Purity
>97.0%(GC)
Density
0.939 g/mL at 25 °C (lit.)
Appearance
Colorless to Light yellow clear liquid
Refractive Index
n20/D 1.444 (lit.)

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
0.9
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
5
Exact Mass
116.083729621 g/mol
Monoisotopic Mass
116.083729621 g/mol
Topological Polar Surface Area
29.5Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
52.5
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114133578-A Filtrate reducer carboxyl hydroxyl modified polyester for drilling fluid 2021-12-30
CN-114133494-A High-performance polycarboxylic acid type water reducing agent, and normal-temperature preparation method, use method and application thereof 2021-12-21
CN-114163464-A Esterification product, low-hydration-heat-ether polycarboxylate superplasticizer and preparation method thereof 2021-12-15
CN-113929895-A Preparation method and application of sodium alkoxide catalyst for synthesizing water reducer polyether 2021-12-08
CN-114015034-A Preparation method and application of sodium alkoxide catalyst for synthesizing water reducer polyether 2021-12-08
CN-113881424-A Composite carbon dioxide fracturing fluid and preparation method thereof 2021-12-07
CN-113881424-B Composite carbon dioxide fracturing fluid and preparation method thereof 2021-12-07
CN-113896842-A Synthetic method of polycarboxylate superplasticizer by taking polyether macromonomer as raw material 2021-11-30
CN-113979661-A Preparation method of nano calcium silicate suspension with high stability and good early strength effect 2021-11-30
CN-114044856-A Mud-blocking type polycarboxylate superplasticizer and preparation method thereof 2021-11-25

Literatures

PMID Publication Date Title Journal
17624362 2007-08-17 Novel in situ polymerized coatings for hydrophobic interaction chromatography media Journal of chromatography. A
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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