CAS Number99-85-4
SynonymsTerpinene; 1-Isopropyl-4-methyl-1,4-cyclohexadiene; MFCD00001537; 1-methyl-4-propan-2-ylcyclohexa-1,4-diene; gamma-terpinene; 1,4-p-Menthadiene; γ-terpinene; 1-Methyl-4-isopropyl-1,4-cyclohexadiene; 1-Methyl-4-(propan-2-yl)cyclohexa-1,4-diene; g-Terpinene; p-Mentha-1,4-diene; 1-Isopropyl-4-methylcyclohexa-1,4-diene; EINECS 202-794-6
Molecular FormulaC10H16
Molecular Weight136.23
Purity97%
Density0.8±0.1 g/cm3
Boiling Point182 °C (lit.)
Melting Point60-61ºC
Appearanceliquid
EINECS202-794-6
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 99-85-4 |
| Catalog No. | 2A-9018156 |
| Chinese Name | γ-松油烯 |
| Synonyms | Terpinene; 1-Isopropyl-4-methyl-1,4-cyclohexadiene; MFCD00001537; 1-methyl-4-propan-2-ylcyclohexa-1,4-diene; gamma-terpinene; 1,4-p-Menthadiene; γ-terpinene; 1-Methyl-4-isopropyl-1,4-cyclohexadiene; 1-Methyl-4-(propan-2-yl)cyclohexa-1,4-diene; g-Terpinene; p-Mentha-1,4-diene; 1-Isopropyl-4-methylcyclohexa-1,4-diene; EINECS 202-794-6 |
| Molecular Formula | C10H16 |
| Molecular Weight | 136.23 |
| Purity | 97 |
| Density | 0.8±0.1 g/cm3 |
| Boiling Point | 182 °C (lit.) |
| Melting Point | 60-61ºC |
| Appearance | liquid |
| Storage Condition | 2-8°C |
| Packaging | III |
| Application | Gamma-terpene, a monoterpenoid, is an orally active antioxidant that directly scavenges free radicals. γ-Terpinene has strong anti-noxious activity [1]. |
| EINECS | 202-794-6 |
| HTC | 2902199090 |
| PubChem ID | 24853370 |
| MDL Number | MFCD00001537 |
| SMILES | CC(C)C1=CCC(C)=CC1 |
| InChI | 1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8H,5-6H2,1-3H3 |
| InChI Key | YKFLAYDHMOASIY-UHFFFAOYSA-N |
| Beilstein/REAXYS | 2038347 |
| NACRES Code | NA.22 |
| eCl@ss | 39010915 |
| UNSPSC | 12352100 |
| Hazard Symbols | 3.2 |
| MSDS | msds/18156_1_99_85_4.pdf |
| Bioactivity | γ-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. γ-Terpinene has potent antinociception activity[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease In Vivo γ-Terpinene (γ-TPN; 12.5, 25 mg/kg; p.o.; single dose) significantly reduces the licking time of the stimulated paw in both phases of the test in male Swiss mice (20-30 g)[1]. γ-Terpinene given either systemically (p.o.; 1.56, 3.125, and 6.25 mg/kg) or centrally (i.t or i.c.v; 10 and 20 μg/site) causes significant inhibition of glutamate-induced nociception in mice[1]. References [1]. Flávia Franceli de Brito Passos, et al. Involvement of Cholinergic and Opioid System in γ-Terpinene-Mediated Antinociception. Evid Based Complement Alternat Med. 2015;2015:829414. [2]. Guo-Xiang Li, et al. Unusual antioxidant behavior of alpha- and gamma-terpinene in protecting methyl linoleate, DNA, and erythrocyte. J Agric Food Chem. 2009 May 13;57(9):3943-8. Chemical & Physical Properties Density 0.8±0.1 g/cm3 Boiling Point 183.0±0.0 °C at 760 mmHg Melting Point 60-61ºC Molecular Formula C10H16 Molecular Weight 136.234 Flash Point 51.7±0.0 °C Exact Mass 136.125198 LogP 4.36 Vapour density 4.7 (vs air) Vapour Pressure 1.1±0.2 mmHg at 25°C Index of Refraction 1.476 InChIKey YKFLAYDHMOASIY-UHFFFAOYSA-N SMILES CC1=CCC(C(C)C)=CC1 Storage condition 2-8°C |
| Use of | γ-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. γ-Terpinene has potent antinociception activity[1]. Properties Articles29 Name γ-terpinene Synonym More Synonyms γ-terpinene Biological Activity Description γ-Terpinene, a monoterpene, is an orally active antioxidant compound which can scavenge radicals directly. γ-Terpinene has potent antinociception activity[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Neurological Disease References [1]. Flávia Franceli de Brito Passos, et al. Involvement of Cholinergic and Opioid System in γ-Terpinene-Mediated Antinociception. Evid Based Complement Alternat Med. 2015;2015:829414. [2]. Guo-Xiang Li, et al. Unusual antioxidant behavior of alpha- and gamma-terpinene in protecting methyl linoleate, DNA, and erythrocyte. J Agric Food Chem. 2009 May 13;57(9):3943-8. Chemical & Physical Properties Molecular Formula C10H16 Exact Mass 136.125198 Vapour density 4.7 (vs air) Index of Refraction 1.476 InChIKey YKFLAYDHMOASIY-UHFFFAOYSA-N SMILES CC1=CCC(C(C)C)=CC1 |
| Tax Rebate | 9.0% |
| Supervision | none |
| Transport Info | Product name: Purity: 0.0% |
| MSDS Transport Info | Module 14. Shipping information 14.1 UN dangerous goods number European Land Transport Danger Regulations: 2319 International Maritime Transport Danger Regulations: 2319 International Air Transport Danger Regulations: 2319 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: TERPENE HYDROCARBONS, N.O.S. IMDG: TERPENE HYDROCARBONS, N.O.S. IMDG: Terpene hydrocarbons, n.o.s. 14.3 Transport hazard categories European land transport Dangerous Regulations: 3 International sea transport Dangerous Regulations: 3 International air transport Dangerous Regulations: 3 14.4 Package group European Land Transport Danger Regulations: III International Maritime Transport Danger Regulations: III International Air Transport Danger Regulations: III 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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