
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.)
Appearanceliquid
EINECS207-889-6
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 499-75-2 |
| Catalog No. | 2A-9022300 |
| Chinese Name | 香芹酚 |
| Synonyms | 5-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 Weight | 150.22 |
| Purity | 98 |
| Density | 1.0±0.1 g/cm3 |
| Boiling Point | 236-237 °C (lit.) |
| Melting Point | 3-4 °C (lit.) |
| Appearance | liquid |
| Water Solubility | Insoluble |
| Storage Condition | Sealed packaging in brown glass bottles. Store in |
| Packaging | III |
| Application | Carvacrol 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 |
| EINECS | 207-889-6 |
| HTC | 2907199090 |
| PubChem ID | 24857025 |
| MDL Number | MFCD00002236 |
| SMILES | CC(C)c1ccc(C)c(O)c1 |
| InChI | 1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4-7,11H,1-3H3 |
| InChI Key | RECUKUPTGUEGMW-UHFFFAOYSA-N |
| Beilstein/REAXYS | 1860514 |
| NACRES Code | NA.22 |
| UNSPSC | 12352100 |
| Hazard Symbols | 8 |
| MSDS | msds/22300_1_499_75_2.pdf |
| Bioactivity | Carvacrol 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 of | Properties 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 Rebate | 9.0% |
| Supervision | None MFN tariff: 5.5% Ordinary tariff: 30.0% |
| Transport Info | Product name: Purity: 0.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
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