4161-24-4 Usage
Description
4-Butoxybutyl alcohol, also known as 4-butoxybutan-1-ol, is an organic compound with the molecular formula C8H18O2. It is a colorless liquid with a mild odor and is soluble in water. 4-Butoxybutyl alcohol is characterized by its hydroxyl and butoxy groups, which contribute to its unique chemical properties and make it suitable for various applications in different industries.
Uses
Used in Biomedical Applications:
4-Butoxybutyl alcohol is used as a key component in the synthesis of biomedical polyurethane. It serves as a building block for creating scaffold materials, which are essential in the field of regenerative medicine and tissue engineering. The alcohol's properties allow for the development of biocompatible and biodegradable scaffolds that can support cell growth and tissue regeneration.
In the Biomedical Industry:
4-Butoxybutyl alcohol is used as a monomer for the production of polyurethane-based scaffolds. These scaffolds are designed to mimic the natural extracellular matrix, providing a supportive structure for cell attachment, proliferation, and differentiation. The alcohol's incorporation into the polyurethane structure enhances the material's biocompatibility, mechanical properties, and degradation rate, making it an ideal candidate for various biomedical applications, such as tissue engineering, drug delivery, and wound healing.
Check Digit Verification of cas no
The CAS Registry Mumber 4161-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4161-24:
(6*4)+(5*1)+(4*6)+(3*1)+(2*2)+(1*4)=64
64 % 10 = 4
So 4161-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O2/c1-2-3-7-10-8-5-4-6-9/h9H,2-8H2,1H3
4161-24-4Relevant articles and documents
Opening of Cyclic Acetals by Trichloro-, Dichloro- and Tribromo-borane
Bonner, Trevor G.,Lewis, David,Rutter, Keith
, p. 1807 - 1810 (2007/10/02)
The rate-determining step in the ring opening of cyclic acetals by trichloroborane to yield α-chloro-ethers is shown to be consistent with the formation of an oxocarbenium ion.Subsequent reduction provides a general route for the conversion of a diol into a hydroxy-ether.Tribromoborane is a more powerful and dichloroborane a less powerful reagent than trichloroborane.
