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316431

Sigma-Aldrich

4-Isopropyl-3-methylphenol

99%

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About This Item

Linear Formula:
(CH3)2CHC6H3(CH3)OH
CAS Number:
3228-02-2
Molecular Weight:
150.22
EC Number:
221-761-7
MDL number:
MFCD00010704
UNSPSC Code:
12352100
PubChem Substance ID:
24859017
NACRES:
NA.22

Assay

99%

form

crystals

mp

111-114 °C (lit.)

SMILES string

CC(C)c1ccc(O)cc1C

InChI

1S/C10H14O/c1-7(2)10-5-4-9(11)6-8(10)3/h4-7,11H,1-3H3

InChI key

IJALWSVNUBBQRA-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8612
STBK3621
STBJ9069
STBJ1649
STBH7166

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Nobuya Magori et al.
European journal of pharmacology, 819, 254-260 (2017-12-12)
Hinokitiol (β-thujaplicin) is a natural tropolone derivative contained in Chamaecyparis taiwanensis that has various actions including anti-inflammatory activities. Various plant-derived compounds inhibit compound action potentials (CAPs) in a manner dependent on the chemical structure of the compounds; however, the effects
Stuart J Lansdell et al.
Molecular pharmacology, 87(1), 87-95 (2014-10-24)
In common with other members of the Cys-loop family of pentameric ligand-gated ion channels, 5-hydroxytryptamine type 3 receptors (5-HT3Rs) are activated by the binding of a neurotransmitter to an extracellular orthosteric site, located at the interface of two adjacent receptor

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