5-Isopropyl-2-methylphenol structure, CAS 499-75-2

5-Isopropyl-2-methylphenol

CAS Number499-75-2

Synonyms5-Isopropyl-o-cresol; 5-Isopropyl-2-Methylphenol; 2-methyl-5-(1-methylethyl)phenol; EINECS 207-889-6; MFCD00002236; 2-methyl-5-propan-2-ylphenol

Molecular Formula(CH3)2CHC6H3(CH3)OH

Molecular Weight150.22

Purity98%

Density1.0±0.1 g/cm3

Boiling Point236-237 °C (lit.)

Melting Point3-4 °C (lit.)

Flash Point

Appearanceliquid

EINECS207-889-6

MSDSChineseEnglish

Symbol8

Signal WordWarning

Cat. No.: 2A-9022300 Purity: 98%
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Quality Control of [ 499-75-2 ] Purity: 98% SDS Specification MoL

Chemical & Physical Properties
CAS Number499-75-2
Catalog No.2A-9022300
Chinese Name香芹酚
Synonyms5-Isopropyl-o-cresol; 5-Isopropyl-2-Methylphenol; 2-methyl-5-(1-methylethyl)phenol; EINECS 207-889-6; MFCD00002236; 2-methyl-5-propan-2-ylphenol
Molecular Formula(CH3)2CHC6H3(CH3)OH
Molecular Weight150.22
Purity98
Density1.0±0.1 g/cm3
Boiling Point236-237 °C (lit.)
Melting Point3-4 °C (lit.)
Appearanceliquid
Water SolubilityInsoluble
Storage ConditionSealed packaging in brown glass bottles. Store in
PackagingIII
ApplicationCarvacrol is a monoterpene phenol from Lamiaceae plants that has antioxidant, anti-inflammatory, and anti-cancer effects. Carvacrol can cause G0/G1 cell cycle arrest, downregulate Notch-1 and Jagged-1
EINECS207-889-6
HTC2907199090
PubChem ID24857025
MDL NumberMFCD00002236
SMILESCC(C)c1ccc(C)c(O)c1
InChI1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3
InChI KeyRECUKUPTGUEGMW-UHFFFAOYSA-N
Beilstein/REAXYS1860514
NACRES CodeNA.22
UNSPSC12352100
Hazard Symbols8
MSDSmsds/22300_1_499_75_2.pdf
BioactivityCarvacrol is a monoterpenoid phenol isolated from Lamiaceae family plants, with antioxidant, anti-inflammatory and anticancer properties. Carvacrol causes cell cycle arrest in G0/G1, downregulates Notch-1, and Jagged-1, and induces apoptosis[1]. Related Catalog Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cancer Signaling Pathways >> Stem Cell/Wnt >> Notch Research Areas >> Inflammation/Immunology References [1]. Khan F, et al. Carvacrol Induced Program Cell Death and Cell Cycle Arrest in Androgen-Independent Human Prostate Cancer Cells via Inhibition of Notch Signaling. Anticancer Agents Med Chem. 2019 Jul 31. Chemical & Physical Properties Density 1.0±0.1 g/cm3 Boiling Point 237.2±9.0 °C at 760 mmHg Melting Point 3-4 °C(lit.) Molecular Formula C10H14O Molecular Weight 150.218 Flash Point 106.7±0.0 °C Exact Mass 150.104462 PSA 20.23000 LogP 3.28 Vapour Pressure 0.0±0.5 mmHg at 25°C Index of Refraction 1.523 InChIKey RECUKUPTGUEGMW-UHFFFAOYSA-N SMILES Cc1ccc(C(C)C)cc1O Stability Stable. Combustible. Incompatible with strong bases, strong oxidizing agents. Water Solubility Insoluble
Use ofProperties Articles53 Name carvacrol Synonym More Synonyms 5-Isopropyl-2-methylphenol Biological Activity Related Catalog Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cancer Signaling Pathways >> Stem Cell/Wnt >> Notch Research Areas >> Inflammation/Immunology References [1]. Khan F, et al. Carvacrol Induced Program Cell Death and Cell Cycle Arrest in Androgen-Independent Human Prostate Cancer Cells via Inhibition of Notch Signaling. Anticancer Agents Med Chem. 2019 Jul 31. Chemical & Physical Properties Molecular Formula C10H14O Exact Mass 150.104462 PSA 20.23000 Index of Refraction 1.523 InChIKey RECUKUPTGUEGMW-UHFFFAOYSA-N Stability Stable. Combustible. Incompatible with strong bases, strong oxidizing agents. Water Solubility Insoluble
Tax Rebate9.0%
SupervisionNone MFN tariff: 5.5% Ordinary tariff: 30.0%
Transport InfoProduct name: Purity: 0.0%
MSDS Transport InfoModule 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified
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