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Merck

T0501

Thymol

≥98.5%

Synonym(s):

2-Isopropyl-5-methylphenol, 5-Methyl-2-(1-methylethyl)phenol, 5-Methyl-2-isopropylphenol, IPMP

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About This Item

Linear Formula:
2-[(CH3)2CH]C6H3-5-(CH3)OH
CAS Number:
Molecular Weight:
150.22
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
EC Number:
201-944-8
Beilstein/REAXYS Number:
1907135
MDL number:

Product Name

Thymol, ≥98.5%

InChI

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

InChI key

MGSRCZKZVOBKFT-UHFFFAOYSA-N

SMILES string

CC(C)c1ccc(C)cc1O

vapor pressure

1 mmHg ( 64 °C)

assay

≥98.5%

form

powder or crystals

bp

232 °C (lit.)

mp

48-51 °C (lit.)

solubility

ethanol: 50 mg/mL

density

0.965 g/mL at 25 °C (lit.)

antibiotic activity spectrum

fungi

application(s)

diagnostic assay manufacturing
hematology
histology

mode of action

DNA synthesis | interferes

storage temp.

room temp

Quality Level

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Application

Thymol is generally added in the Hematoxylin and Eosin staining solution to prevent mould growth. It is also suitable for use in antimicrobial screening by the disk diffusion method. It has been used as a test compound in antifungal assay to assess the susceptibility of various fungal isolates.

Disclaimer

The product is not intendedfor use as a biocide under global biocide regulations, including but notlimited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, EuropeanBiocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’sBiocidal Products Regulation, Korea’s Consumer Chemical Products and BiocideSafety Management Act (K-BPR) and others.

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

240.8 °F - closed cup

flash_point_c

116 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Olivier Duverger et al.
Journal of cellular physiology, 228(3), 654-664 (2012-08-14)
Mutations in DLX3 in humans lead to defects in craniofacial and appendicular bones, yet the in vivo activities related to Dlx3 function during normal skeletal development have not been fully elucidated. Here we used a conditional knockout approach to analyze
Sandeep Sharma et al.
Antimicrobial agents and chemotherapy, 53(1), 216-222 (2008-06-25)
Hydroxychavicol isolated from the chloroform extraction of aqueous extract of Piper betle leaves showed inhibitory activity against oral cavity pathogens. It exhibited an inhibitory effect on all of the oral cavity pathogens tested (MICs of 62.5 to 500 microg/ml) with
Hiroko Ohwada et al.
Research in developmental disabilities, 34(1), 650-655 (2012-11-06)
As the life expectancy of people with intellectual disability (ID) increases, it is becoming necessary to understand factors affecting survival. However, predictors that are typically assessed among healthy people have not been examined. Predictors of all-cause mortality, including blood, urine
Poliana Guerino Marson Ascêncio et al.
Evidence-based complementary and alternative medicine : eCAM, 2014, 190543-190543 (2015-01-15)
Costus spiralis (Costaceae) is a species native to the Amazon region and is used in traditional medicine. The endophytic fungi used in this study were obtained from leaves of this plant. 13 strains were selected to obtain hydroethanolic extracts and
H Hashemipour et al.
Poultry science, 92(8), 2059-2069 (2013-07-23)
This trial was conducted to evaluate the effects of dietary supplementation of phytogenic product containing an equal mixture of thymol and carvacrol at 4 levels (0, 60, 100, and 200 mg/kg of diet) on performance, antioxidant enzyme activities, fatty acid

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