CAS 13466-78-9
:3-Carene
Descrizione:
3-Carene è un monoterpene biciclico caratterizzato dalla sua struttura unica, che include un anello a sei membri fuso a un anello a cinque membri. È un liquido incolore a temperatura ambiente e possiede un aroma distintivo dolce e simile al pino, rendendolo un composto prezioso nelle industrie delle fragranze e dei sapori. La formula molecolare di 3-Carene è C10H16, ed è noto per la sua volatilità e natura idrofobica. Questo composto si trova comunemente in vari oli essenziali, in particolare in specie di pino e cedro, ed è spesso utilizzato come solvente e nella sintesi di altri composti organici. 3-Carene mostra una reattività chimica interessante, inclusa la capacità di subire ossidazione e polimerizzazione. Inoltre, è stato studiato per le sue potenziali attività biologiche, comprese proprietà anti-infiammatorie e antimicrobiche. La sua presenza in prodotti naturali e le sue applicazioni in varie industrie evidenziano la sua importanza sia in chimica che negli usi pratici.
Formula:C10H16
InChI:InChI=1/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m0/s1
InChI key:InChIKey=BQOFWKZOCNGFEC-UHFFFAOYSA-N
SMILES:CC1(C)C2C1CC(C)=CC2
Sinonimi:- (.+-.)-Δ3-Carene
- (1R,6S)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene
- (±)-Δ<sup>3</sup>-Carene
- 3,7,7-Trimethylbicyclo[4.1.0]hept-3-en
- 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
- 3,7,7-Trimetilbiciclo[4.1.0]Hept-3-Eno
- 3-Carene (delta)
- Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-
- delta-3-Carene
- δ-3-CARENE
- 3-Carene
- 3-Norcarene, 3,7,7-trimethyl-
- 3-Carene, stabilized, 90% 1LT
- delta-3-CARENE, NATURAL
- S-3-Carene
- 3-Carene, stabilized, 90% 25ML
- 3-Carene, stabilized, 90%
- carene
- Isodiprene
- 3,7,7-trimethyl-3-norcaren
- δ3-Carene, 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
- 3-delta-carene
- delta(Sup3)-Carene
- 3-Karen
- 3-CARVENE
- 4,7,7-Trimethyl-3-norcarene
- 3,7,7-Trimethylbicyclo(4.1.0)hept-3-ene for synthesis
- DELTA-CARENE
- FEMA 3821
- Car-3-ene
- 3,7,7-trimethyl-bicyclo[4.1.0]hept-3-en
- 3-Carene 90%
- 3-Carene,δ3-Carene, 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
- 3,7,7-TRIMETHYLBICYCLO[4.1.0]-3-HEPTENE
- CARENE, DELTA-3
- 3,7,7-Trimethyl-3-norcarene
- δ-3-carene,3,7,7-trimethylbicyclohept-3-ene
- 3-Carene,90%,stabilized
- CARENE, Delta-3-(SG)
- D-CARENE
- 3-Karen (jfr terpener)
- 3-CARENE WITH GC
- 3,7,7-trimethyl-bicyclo(4.1.0)hept-3-en
- CAREN-(3), ROH
- Vedi altri sinonimi
Ordinare per
Purezza (%)
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100
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0
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50
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90
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95
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100
17 prodotti.
3-Carene
CAS:3-Carene analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C10H16Purezza:(GC) ≥90% (sum of enantiomers)Colore e forma:LiquidPeso molecolare:136.243,7,7-Trimethylbicyclo[4.1.0]Hept-3-Ene
CAS:<p>3,7,7-Trimethylbicyclo[4.1.0]Hept-3-Ene</p>Purezza:95%Peso molecolare:136.23g/molSmart Solutions™ TerpiMix Kit 2500 μg/mL in Isopropanol
CAS:Prodotto controllato- 10458-14-7
- 105-87-3
- 106-22-9
- 106-24-1
- 106-25-2
- 111-02-4
- 112-14-1
- 1139-30-6
- 116-26-7
- 1196-01-6
- 123-35-3
- 124-76-5
- 125-12-2
- 127-91-3
- 13466-78-9
- 138-86-3
- 13877-91-3
- 2217-02-9
- 2244-16-8
- 22567-21-1
- 3387-41-5
- 4602-84-0
- 4630-07-3
- 464-43-7
- 464-45-9
- 4674-50-4
- 469-61-4
- 4695-62-9
- 470-82-6
- 489-86-1
- 498-15-7
- 499-75-2
- 502-61-4
- 515-69-5
- 527-84-4
- 535-77-3
- 5392-40-5
- 546-79-2
- 546-80-5
- 562-74-3
- 586-62-9
- 638-36-8
- 675-20-7
- 6753-98-6
- 7212-44-4
- 7541-49-3
- 76-22-2
- 77-53-2
- 7787-20-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-78-1
- 89-79-2
- 89-81-6
- 89-82-7
- 89-83-8
- 98-55-5
- 99-83-2
- 99-85-4
- 99-86-5
- 99-87-6
Colore e forma:KitCanada Terpene Mixture 1 2500 µg/mL in Hexane
CAS:- 106-24-1
- 123-35-3
- 13466-78-9
- 13877-91-3
- 18172-67-3
- 23089-26-1
- 489-86-1
- 586-62-9
- 5989-27-5
- 6753-98-6
- 7212-44-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-79-2
- 99-85-4
- 99-86-5
- 99-87-6
Formula:C10H16Colore e forma:MixturePeso molecolare:136.23Canada Terpene Mixture 1 2500 µg/mL in Hexane
CAS:- 106-24-1
- 123-35-3
- 13466-78-9
- 13877-91-3
- 18172-67-3
- 23089-26-1
- 489-86-1
- 586-62-9
- 5989-27-5
- 6753-98-6
- 7212-44-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-79-2
- 99-85-4
- 99-86-5
- 99-87-6
Formula:C10H16Colore e forma:MixturePeso molecolare:136.23Cannabis Terpene Mixture 1 2500 µg/mL in Hexane
CAS:Prodotto controllato- 106-24-1
- 123-35-3
- 13466-78-9
- 13877-91-3
- 18172-67-3
- 23089-26-1
- 489-86-1
- 586-62-9
- 5989-27-5
- 6753-98-6
- 7212-44-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-79-2
- 99-85-4
- 99-86-5
- 99-87-6
Formula:C10H16Colore e forma:MixturePeso molecolare:136.23Cannabis Terpene Mixture 1 2500 ug/mL in Hexane
CAS:Prodotto controllato- 106-24-1
- 123-35-3
- 13466-78-9
- 13877-91-3
- 18172-67-3
- 23089-26-1
- 489-86-1
- 586-62-9
- 5989-27-5
- 6753-98-6
- 7212-44-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-79-2
- 99-85-4
- 99-86-5
- 99-87-6
Formula:C10H16Colore e forma:MixturePeso molecolare:136.233-Carene
CAS:<p>3-Carene(Delta-3-Carene) is a bicyclic monoterpene extracted from western larch and Douglas-fir that acts as a phytofungicide.3-Carene inhibits inflammatory</p>Formula:C10H16Purezza:92.18%Colore e forma:Conform To Requirements Of Company (Method Drt 6903) Liquid LiquidPeso molecolare:136.23Ref: 4Z-T-147003
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta3-Carene
CAS:Prodotto controllato<p>Applications 3-Carene is a mutagenic compound that may be found in the fumes of heating freshly cut spruce and birch chips. 3-Carene is also found i many esential oils and it inhibits acetylcholinesterase activity.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Kurttio, P., et. al.: Mutat. Res., 242, 9 (1990); Miyazawa, M., Yamafuji, C.: J. Arg. Food Chem., 53, 1765 (2005)<br></p>Formula:C10H16Colore e forma:ColourlessPeso molecolare:136.23δ-3-Carene
CAS:<p>δ-3-Carene is an α, β-unsaturated ketone that is produced by the cytochrome P450 enzyme. It can be found in a number of plants and oils, including peppermint, eucalyptus, and pine oil. δ-3-Carene has been shown to have synergistic effects with chemical pesticides such as permethrin when applied in combination. The chemical structure of δ-3-carene is asymmetric and it can be synthesized using a variety of experimental methods. The reaction mechanism for the production of δ-3-carene is unclear but most likely involves a chemical reaction between anhydrous sodium and an organic compound such as acetone or methanol. This reaction releases water vapor from the organic compound and generates heat.</p>Formula:C10H16Purezza:90%MinColore e forma:Clear LiquidPeso molecolare:136.23 g/mol









