(-)-ISOCARYOPHYLLENE

Product Name: (-)-ISOCARYOPHYLLENE
CAS No.: 118-65-0
Chemical Name: (-)-ISOCARYOPHYLLENE
Synonyms: BETA-CARYOPHYLLENE;Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-,[1R-(1R*,4Z,9S*)]-;(Z)-beta-caryophyllene;Bicyclo7.2.0undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4Z,9S)-;(1R,4Z,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene;4,11,11-trimethyl-8-methylene-,[1R-(1R*,4Z,9S*)]-Bicyclo[7.2.0]undec-4-ene;,9s)]-;(-)-ISOCARYOPHYLLENE;(-)-ISOCARYOPHYLLENE;ISOCARYOPHYLLENE, (-)-
CBNumber: CB7730612
Molecular Formula: C15H24
Formula Weight: 204.35
MOL File: 118-65-0.mol

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(-)-ISOCARYOPHYLLENE Property

Melting point:: 25°C
Boiling point:: 271-273 °C(lit.)
alpha: D -24° (chloroform)
Density: 0.893 g/mL at 20 °C(lit.)
refractive index: n20/D 1.496
Flash point:: 215 °F
storage temp.: 2-8°C
solubility: Chloroform (Slightly), Methanol (Slightly)
form: Oil
color: Colourless
Odor: at 100.00 %. woody spicy
Odor Type: woody
Stability:: Light Sensitive
LogP: 6.416 (est)
EPA Substance Registry System: Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4Z,9S)- (118-65-0)

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Safety

Safety Statements: 23-24/25
WGK Germany: 3
F: 10-23

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC

Product number: I789400
Product name: Isocaryophyllene(80%)
Packaging: 100mg
Price: $185
Updated: 2021/12/16

Usbiological

Product number: 452551
Product name: Isocaryophyllene
Packaging: 100mg
Price: $460
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CCH0007057
Product name: (-)-ISOCARYOPHYLLENE
Purity: 95.00%
Packaging: 5MG
Price: $495.77
Updated: 2021/12/16

Medical Isotopes, Inc.

Product number: 65653
Product name: Isocaryophyllene
Packaging: 500mg
Price: $650
Updated: 2021/12/16

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(-)-ISOCARYOPHYLLENE Chemical Properties,Usage,Production

Uses

Isocaryophyllene is an Z- isomer of β-Caryophyllene (C184725). β-Caryophyllene is one of the chemical compounds that contributes to the spiciness of black pepper. β-Caryophyllene was shown to selectively bind to the cannabinoid receptor type-2 (CB2) and to exert significant cannabimimetic antiinflammatory effects in mice.

Uses

In perfumery.

Definition

ChEBI: Isocaryophyllene is a sesquiterpenoid.

Purification Methods

Purify it by vacuum distillation or GLC using a nitrile-silicone column [Corey et al. J Am Chem Soc 86 485 1964, Ramage & Simonsen J Chem Soc 741 1936, Kumar et al.Synthesis 461 1976]. [Beilstein 5 III 1085.]

(-)-ISOCARYOPHYLLENE Preparation Products And Raw materials

Raw materials

Preparation Products

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(-)-ISOCARYOPHYLLENE Suppliers

China 9 Czech 1 France 1 Germany 1 India 4 Switzerland 1 United Kingdom 1 United States 4 Global 22

Interchim S.A.

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118-65-0, (-)-ISOCARYOPHYLLENERelated Search:

(-)-beta-Caryophyllene epoxide,beta-Caryophyllene oxide beta-caryophyllene alcohol Isocaryophyllene oxide β-Caryophyllene ISOCARYOPHYLLENE, (-)-(SG) (-)-ISOCARYOPHYLLENE Beta-Caryophyllene

,9s)]-

4,11,11-trimethyl-8-methylene-,[1R-(1R*,4Z,9S*)]-Bicyclo[7.2.0]undec-4-ene

Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-,[1R-(1R*,4Z,9S*)]-

(1R,4Z,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene

bicyclo[7.2.0]undec-4-ene,4,11,11-trimethyl-8-methylene-,[1theta-(1theta,4z

(-)-ISOCARYOPHYLLENE

ISOCARYOPHYLLENE, (-)-

BETA-CARYOPHYLLENE

(1R,9S)-8-METHYLEN-4,11,11-TRIMETHYL-BICYCLO[7.2.0]UNDEC-4-ENE

(1R,9S,4Z)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene

[1R,4Z,9S,(-)]-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene

(1r-(1r*,4z,9s*))-4,11,11-trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene

(1r-(1r,4z,9s))-4,11,11-trimethyl

(1r-(1r,4z,9s))-4,11,11-trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene

(Z)-beta-caryophyllene

Bicyclo7.2.0undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4Z,9S)-

4,11,11-trimethyl-8-methylene-, [1R-(1R*,4Z,9S*)]-Bicyclo[7.2.0]undec-4-ene bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1 theta-(1 theta,4z ,9s)]- (-)-isocaryophyllene

(-)-ISOCARYOPHYLLENE

Eugenol Impurity 28 (Isocaryophyllene)

Picosulfate Disodium Said

118-65-0

Asymmetric Synthesis

Organic Building Blocks

Alkenes

Chiral Building Blocks

pharmacetical