CAS Number13466-78-9
Synonyms(±)-D3-Carene; 3-Carene,stabilized; 4,7,7-Trimethyl-3-norcarene; MFCD00001315; 3-δ-Carene; 3,7,7-trimethyl-bicyclo[4.1.0]hept-3-ene; 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene; d3-carene; (±)-3-Carene; 3-carene; EINECS 236-719-3; carene; δ3-Carene; Isodiprene
Molecular FormulaC10H16
Molecular Weight136.234
Purity98%%
Density0.9±0.1 g/cm3
Boiling Point171.4±0.0 °C at 760 mmHg
Melting Point25°C
AppearanceLiquid | Clear colorless to slightly yellow
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 13466-78-9 |
| Catalog No. | 2A-1172208 |
| Chinese Name | 3-蒈烯 |
| Synonyms | (±)-D3-Carene; 3-Carene,stabilized; 4,7,7-Trimethyl-3-norcarene; MFCD00001315; 3-δ-Carene; 3,7,7-trimethyl-bicyclo[4.1.0]hept-3-ene; 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene; d3-carene; (±)-3-Carene; 3-carene; EINECS 236-719-3; carene; δ3-Carene; Isodiprene |
| Molecular Formula | C10H16 |
| Molecular Weight | 136.234 |
| Purity | 98% |
| Density | 0.9±0.1 g/cm3 |
| Boiling Point | 171.4±0.0 °C at 760 mmHg |
| Melting Point | 25°C |
| Appearance | Liquid | Clear colorless to slightly yellow |
| Storage Condition | Warehouse low temperature ventilation and drying |
| Packaging | III |
| Application | 3-Carene is a bicyclic monoterpene compound found in pine essential oil. 3-Carene can inhibit inflammatory infiltration and COX-2 overexpression caused by pain stimulation, and has anti-nociceptive ef |
| HTC | 2902199090 |
| PubChem ID | 3155643 |
| SMILES | CC1=CCC2C(C1)C2(C)C |
| InChI | InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3 |
| InChI Key | InChIKey=BQOFWKZOCNGFEC-UHFFFAOYSA-N |
| Hazard Symbols | 3.2 |
| MSDS | msds/172446_2_13466_78_9.pdf |
| Bioactivity | 3-Carene is a bicyclic monoterpene in essential oils extracted from pine trees. 3-Carene inhibits nociceptive stimulus-induced inflammatory infiltrates and COX-2 overexpression, and with antinociceptive effect. 3-Carene stimulates the activity and expression of alkaline phosphatase that is an early phase marker of osteoblastic differentiation[1][2]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology References [1]. Huang XL, e tal. Anti-inflammatory and antinociceptive effects of active ingredients in the essential oils from Gynura procumbens, a traditional medicine and a new and popular food material.J Ethnopharmacol. 2019 Jul 15;239:111916. [2]. Jeong JG, et al. Low concentration of 3-carene stimulates the differentiation of mouse osteoblastic MC3T3-E1 subclone 4 cells. Phytother Res. 2008 Jan;22(1):18-22. Chemical & Physical Properties Density 0.9±0.1 g/cm3 Boiling Point 171.4±0.0 °C at 760 mmHg Melting Point 25°C Molecular Formula C10H16 Molecular Weight 136.234 Flash Point 46.1±0.0 °C Exact Mass 136.125198 LogP 4.37 Appearance of Characters Liquid | Clear colorless to slightly yellow Vapour Pressure 1.9±0.1 mmHg at 25°C Index of Refraction 1.479 Stability Stable. Flammable. Incompatible with strong oxidizing agents. |
| Use of | 3-Carene is a bicyclic monoterpene in essential oils extracted from pine trees. 3-Carene inhibits nociceptive stimulus-induced inflammatory infiltrates and COX-2 overexpression, and with antinociceptive effect. 3-Carene stimulates the activity and expression of alkaline phosphatase that is an early phase marker of osteoblastic differentiation[1][2]. Properties Articles31 Name car-3-ene Synonym More Synonyms carene Biological Activity Description 3-Carene is a bicyclic monoterpene in essential oils extracted from pine trees. 3-Carene inhibits nociceptive stimulus-induced inflammatory infiltrates and COX-2 overexpression, and with antinociceptive effect. 3-Carene stimulates the activity and expression of alkaline phosphatase that is an early phase marker of osteoblastic differentiation[1][2]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Inflammation/Immunology References [1]. Huang XL, e tal. Anti-inflammatory and antinociceptive effects of active ingredients in the essential oils from Gynura procumbens, a traditional medicine and a new and popular food material.J Ethnopharmacol. 2019 Jul 15;239:111916. Chemical & Physical Properties Molecular Formula C10H16 Exact Mass 136.125198 Appearance of Characters Liquid | Clear colorless to slightly yellow Index of Refraction 1.479 Stability Stable. Flammable. Incompatible with strong oxidizing agents. |
| Tax Rebate | 9.0% |
| Supervision | none |
| Transport Info | Shipping Name: UN |
| 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 United Nations shipping name 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 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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