CAS Number98-55-5
SynonymsTERPINENOL; 2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol; alpha-terpineol; pc593; MFCD00001557; TILIANOL NP; A-TERPINEOL; EINECS 232-268-1; TERPINEOL BP; TERPINEOL N; Terpineol schlechthin; Terpenol; p-menth-1-en-8-ol; L6UTJ A1 DXQ1&1; α-Terpineol; Terpilenol
Molecular FormulaC10H18O
Molecular Weight154.25
Purity90%
Density0.9±0.1 g/cm3
Boiling Point217-218 °C (lit.)
Melting Point31-35 °C (lit.)
AppearanceColorless to light yellow crystals
EINECS233-986-8
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 98-55-5 |
| Catalog No. | 2A-9018072 |
| Chinese Name | alpha-松油醇 |
| Synonyms | TERPINENOL; 2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol; alpha-terpineol; pc593; MFCD00001557; TILIANOL NP; A-TERPINEOL; EINECS 232-268-1; TERPINEOL BP; TERPINEOL N; Terpineol schlechthin; Terpenol; p-menth-1-en-8-ol; L6UTJ A1 DXQ1&1; α-Terpineol; Terpilenol |
| Molecular Formula | C10H18O |
| Molecular Weight | 154.25 |
| Purity | 90 |
| Density | 0.9±0.1 g/cm3 |
| Boiling Point | 217-218 °C (lit.) |
| Melting Point | 31-35 °C (lit.) |
| Appearance | Colorless to light yellow crystals |
| Water Solubility | negligible |
| Storage Condition | Store in a cool, ventilated warehouse. Keep away f |
| Application | α-Terpineol is isolated from Eucalyptus globulus Labill and has strong antibacterial activity against periodontal disease and cariogenic bacteria. α-Terpineol has antifungal activity against T. mentag |
| EINECS | 233-986-8 |
| HTC | 29061400 |
| PubChem ID | 24867093 |
| MDL Number | MFCD00001557 |
| SMILES | CC1=CC[C@H](CC1)C(C)(C)O |
| InChI | 1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3 |
| InChI Key | WUOACPNHFRMFPN-UHFFFAOYSA-N |
| Beilstein/REAXYS | 2325137 |
| NACRES Code | NA.22 |
| UNSPSC | 12352212 |
| Hazard Symbols | Transport |
| MSDS | msds/18072_1_98_55_5.pdf |
| Bioactivity | α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1].α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. Related Catalog Research Areas >> Infection Research Areas >> Inflammation/Immunology Signaling Pathways >> Anti-infection >> Bacterial References [1]. Park SN, et al. Antimicrobial effect of linalool and α-terpineol against periodontopathic and cariogenic bacteria. Anaerobe. 2012 Jun;18(3):369-72. [2]. Park MJ, et al. Effect of citral, eugenol, nerolidol and alpha-terpineol on the ultrastructural changes of Trichophyton mentagrophytes. Fitoterapia. 2009 Jul;80(5):290-6. Chemical & Physical Properties Density 0.9±0.1 g/cm3 Boiling Point 217.5±0.0 °C at 760 mmHg Melting Point 31-34ºC Molecular Formula C10H18O Molecular Weight 154.249 Flash Point 89.4±0.0 °C Exact Mass 154.135757 PSA 20.23000 LogP 2.79 Vapour Pressure 0.0±0.9 mmHg at 25°C Index of Refraction 1.483 InChIKey WUOACPNHFRMFPN-UHFFFAOYSA-N SMILES CC1=CCC(C(C)(C)O)CC1 Storage condition 2-8°C Water Solubility negligible |
| Use of | α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1].α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. Properties Articles34 Name α-terpineol Synonym More Synonyms Terpineol Biological Activity Description α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1].α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. Related Catalog Research Areas >> Infection Research Areas >> Inflammation/Immunology Signaling Pathways >> Anti-infection >> Bacterial References [1]. Park SN, et al. Antimicrobial effect of linalool and α-terpineol against periodontopathic and cariogenic bacteria. Anaerobe. 2012 Jun;18(3):369-72. [2]. Park MJ, et al. Effect of citral, eugenol, nerolidol and alpha-terpineol on the ultrastructural changes of Trichophyton mentagrophytes. Fitoterapia. 2009 Jul;80(5):290-6. Chemical & Physical Properties Molecular Formula C10H18O Exact Mass 154.135757 PSA 20.23000 Index of Refraction 1.483 InChIKey WUOACPNHFRMFPN-UHFFFAOYSA-N SMILES CC1=CCC(C(C)(C)O)CC1 Water Solubility negligible |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 5.5%. Ordinary tariff: 30.0% |
| Transport Info | Shipping Name: UN |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available |
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