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Merck

T0501

Thymol

≥98.5%

Synonyme(s) :

5-méthyl-2-(1-méthyléthyl)phénol, 5-méthyl-2-isopropylphénol

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A propos de cet article

Formule linéaire :
2-[(CH3)2CH]C6H3-5-(CH3)OH
Numéro CAS:
89-83-8
Poids moléculaire :
150.22
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
57654643
EC Number:
201-944-8
Beilstein/REAXYS Number:
1907135
MDL number:
MFCD00002309

Principaux documents

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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

200

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Catégories apparentées

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

Classe de stockage

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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Certificats d'analyse (COA)

Lot/Batch Number
0000527811
0000527811
0000527810
0000527810
0000515938

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Consulter la Bibliothèque de documents

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
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
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
S P Lee et al.
British journal of pharmacology, 153(8), 1739-1749 (2008-03-13)
Thymol, a major component of thyme and oregano, has medical uses in oral care products as an astringent and antibiotic. Its distinctive sharp odour and pungent flavour are considered aversive properties. The molecular basis of these aversive properties is not
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
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