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About This Item
Empirical Formula (Hill Notation):
C10H18O2
CAS Number:
Molecular Weight:
170.25
UNSPSC Code:
12162002
EC Number:
269-768-4
InChI key
GGAXPLCKKANQED-UHFFFAOYSA-N
InChI
1S/C10H18O2/c1-7(2)9-5-4-8(3)6-10(11)12-9/h7-9H,4-6H2,1-3H3
assay
≥98.0%
form
liquid
color
colorless to pale yellow
storage temp.
−20°C
General description
Menthide is a seven-membered, plant-derived lactone monomer that can be readily polymerized via ring opening polymerization (ROP). Controlled ROP has yielded aliphatic polyesters with high molecular weights and narrow molecular weight distributions (PDI). Menthide has been copolymerized with other biologically derived monomers, such as lactide, to yield products such as thermoplastic elastomers and pressure-sensitive adhesives.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Polyurethanes based on renewable polyols from bioderived lactones.
Gurusamy-Thangavelu SA, et al.
Polym. Chem., 3, 2941-2948 (2012)
James A Wilson et al.
Biomacromolecules, 16(10), 3191-3200 (2015-09-18)
We report the one-pot copolymerization of ω-pentadecalactone (PDL) to produce tri- and diblock-like copolymers with the ability to undergo postpolymerization modification. The ε-substituted ε-lactone (εSL), menthide (MI), was copolymerized with PDL to introduce side chain functionality into poly(ω-pentadecalactone) (PPDL) copolymers.
Jihoon Shin et al.
Biomacromolecules, 13(11), 3833-3840 (2012-10-16)
Renewable ABA triblock copolymers were prepared by sequential polymerization of the plant-based monomers menthide and α-methylene-γ-butyrolactone (MBL or tulipalin A). Ring-opening transesterification polymerization of menthide using diethylene glycol as an initiator gave α,ω-dihydroxy poly(menthide) (HO-PM-OH), which was converted to α,ω-dibromo
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