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Merck
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Documentos

75541

Supelco

(−)-trans-Caryophyllene

analytical standard

Sinónimos:

β-Caryophyllene, trans-(1R,9S)-8-Methylene-4,11,11-trimethylbicyclo[7.2.0]undec-4-ene

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About This Item

Fórmula empírica (notación de Hill):
C15H24
Número de CAS:
87-44-5
Peso molecular:
204.35
Beilstein:
2044564
Número CE:
201-746-1
Número MDL:
MFCD00075925
Código UNSPSC:
85151701
ID de la sustancia en PubChem:
329766500
NACRES:
NA.24

grado

analytical standard

Nivel de calidad

100

Análisis

≥98.0% (sum of enantiomers, GC)

actividad óptica

[α]20/D -10±1°, neat

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

bp

262-264 °C (lit.)

densidad

0.902 g/mL at 20 °C (lit.)

aplicaciones

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

[H][C@@]12CC\C(C)=C\CCC(=C)[C@H]1CC2(C)C

InChI

1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6+/t13-,14-/m1/s1

Clave InChI

NPNUFJAVOOONJE-GFUGXAQUSA-N

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Aplicación

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Otras notas

This compound is commonly found in plants of the genus: cinnamomum melissa

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palabra de señalización

Danger

Frases de peligro

H304,H317

Clasificaciones de peligro

Asp. Tox. 1 - Skin Sens. 1B

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

221.9 °F - closed cup

Punto de inflamabilidad (°C)

105.5 °C - closed cup

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCG8176
BCCF5013
BCCC3373
BCCB4774
BCBZ5011

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USP

1268965

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o-Cymene 98%

Sigma-Aldrich

255270

o-Cymene

Louis M T Bradbury et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(27), E1888-E1897 (2012-06-19)
In photosynthetic organisms, carotenoids serve essential roles in photosynthesis and photoprotection. A previous report designated CruP as a secondary lycopene cyclase involved in carotenoid biosynthesis [Maresca J, et al. (2007) Proc Natl Acad Sci USA 104:11784-11789]. However, we found that
Pablinny Moreira Galdino et al.
Progress in neuro-psychopharmacology & biological psychiatry, 38(2), 276-284 (2012-05-01)
Spiranthera odoratissima A. St. Hil. (manacá) is used in folk medicine to treat renal and hepatic diseases, stomachache, headaches and rheumatism. A central nervous system (CNS) depressant effect of the hexane fraction from the ethanolic extract of this plant has
Rajesh K Joshi
Natural product communications, 8(3), 401-402 (2013-05-18)
The essential oil composition from the aerial parts of Baccharoides lilacina (Dalzell & A. Gibson) M. R. Almeida was analyzed by gas chromatography (GC) and gas chromatography/mass spectrometry (GC/MS). A total of 41 compounds have been identified, representing 97.4% of
S Katsuyama et al.
European journal of pain (London, England), 17(5), 664-675 (2012-11-10)
β-caryophyllene (BCP) is a common constitute of the essential oils of numerous spice, food plants and major component in Cannabis. The present study investigated the contribution of peripheral cannabinoid (CB) and opioid systems in the antinociception produced by intraplantar (i.pl.)
Tamara van Molken et al.
Oecologia, 170(2), 433-444 (2012-04-25)
Plant pathogens and insect herbivores are prone to share hosts under natural conditions. Consequently, pathogen-induced changes in the host plant can affect herbivory, and vice versa. Even though plant viruses are ubiquitous in the field, little is known about plant-mediated
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