ChemicalBook--->CAS DataBase List--->4621-04-9

4621-04-9

4621-04-9 Structure

4621-04-9 Structure
IdentificationBack Directory
[Name]

4-ISO-PROPYLCYCLOHEXANOL
[CAS]

4621-04-9
[Synonyms]

APO PATCHONE
APOPATCHONE, IFF
Folrosia 5094001
TIMTEC-BB SBB008023
4-ISPROPYLCYCLOHEXANOL
Isopropyl cyclohexanol
p-isopropyl-cyclohexano
P-ISOPROPYL CYCLOHEXANOL
4-ISO-PROPYLCYCLOHEXANOL
Isopropylcyclohexanol, p-
4-ISPROPYLCYCLOHEXANOL 95%
Cyclohexanol, 4-isopropyl-
Cyclohexanol, p-isopropyl-
PARA ISOPROPYL CYCLOHEXANOL
4-propan-2-ylcyclohexan-1-ol
4-(1-methylethyl)-cyclohexano
4-(1-methylethyl)-Cyclohexanol
Cyclohexanol, 4-(1-methylethyl)-
4-Isopropylcyclohexanol (Isomer 1)
4-Isopropylcyclohexanol (Isomer 2)
4-Isopropylcyclohexanol(cis-andtrans-mixture)>
4-Isopropylcyclohexanol (cis- and trans- mixture)
4-Isopropylcyclohexanol (cis- andtrans- Mixture)
4-Isopropylcyclohexanol (cis- andtrans- Mixture)
4-ISO-PROPYLCYCLOHEXANOL ---99% ISOMER MIXTURE, D25 0.916, N20 1.4679---
[EINECS(EC#)]

225-035-0
[Molecular Formula]

C9H18O
[MDL Number]

MFCD00043476
[MOL File]

4621-04-9.mol
[Molecular Weight]

142.24
Chemical PropertiesBack Directory
[Melting point ]

36.9°C (estimate)
[Boiling point ]

110°C/22mmHg(lit.)
[density ]

0.9103 (estimate)
[vapor pressure ]

4.73-6.3Pa at 20-25℃
[refractive index ]

gt. 1.4660 to 1.4700
[Fp ]

95 °C
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[pka]

15.30±0.40(Predicted)
[color ]

Colorless to Almost colorless
[Odor]

at 10.00 % in dipropylene glycol. leather red rose green dusty weedy metallic
[Odor Type]

leathery
[LogP]

2.7-2.8 at 35℃
[Surface tension]

36.7mN/m at 1g/L and 20℃
[EPA Substance Registry System]

Cyclohexanol, 4-(1-methylethyl)- (4621-04-9)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

26-39
[RTECS ]

GV9620000
[HS Code ]

2906190090
Hazard InformationBack Directory
[Biochem/physiol Actions]

4-isopropylcyclohexanol (4-iPr-CyH-OH), a novel analgesic compound ,  which inhibited TRPV1, TRPA1, TRPM8, TRPV4 and ANO1, as well as mitigated capsaicin-induced pain-related behaviors in mice. Moreover, the absence of an agonist effect for 4-iPr-CyH-OH on these five channels may reduce side effects and dosages[1].
[References]

[1] Yasunori Takayama, M. Tominaga, H. Furue. “4-isopropylcyclohexanol has potential analgesic effects through the inhibition of anoctamin 1, TRPV1 and TRPA1 channel activities.” Scientific Reports (2017).
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