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Merck

442505

Supelco

Camphene

analytical standard

Sinónimos:

DL-Camphene

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About This Item

Fórmula empírica (notación de Hill):
C10H16
Número de CAS:
Peso molecular:
136.23
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

Quality Level

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

159-160 °C (lit.)

mp

48-52 °C (lit.)

density

0.85 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

storage temp.

2-30°C

SMILES string

[H][C@]12CC[C@]([H])(C1)C(C)(C)C2=C

InChI

1S/C10H16/c1-7-8-4-5-9(6-8)10(7,2)3/h8-9H,1,4-6H2,2-3H3/t8-,9+/m0/s1

InChI key

CRPUJAZIXJMDBK-DTWKUNHWSA-N

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General description

Camphene is an organic plastic type of crystal, which can be commonly used as an industrial intermediate compound for the production of commercial chemicals like camphor, isobornyl acetate and isoborneol. It can be obtained, via isomerization of alpha-pinene over acidic titanium dioxide catalyst.
Camphene offers an extensive and rapidly growing portfolio of analytical standards of active ingredients and marker compounds for a wide range medicinal plants used in herbal medicinal products, nutraceuticals and research. Camphene, a cyclic monoterpene is identified as an important constituent of the essential oils of Piper hymenophyllum Miq, Apiaceae species, Xanthium strumarium L., etc. It is also reportedly known as a fragrance ingredient in Rosa hybrida, Stanhopea orchid species, etc. Camphene is reported to be used in perfume industry with its natural source being Lamiaceae (Satureja douglasii).

Application

Camphene may be used as an analytical reference standard for the quantification of the analyte in Rosa hybrida and fish samples using gas chromatography coupled to mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Flam. Sol. 1

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 2

flash_point_f

78.8 °F - DIN 51755 Part 1

flash_point_c

26 °C - DIN 51755 Part 1

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificados de análisis (COA)

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Los clientes también vieron

Slide 1 of 3

1 of 3

Phytochemical composition and in vitro antimicrobial activity of essential oil of Piper hymenophyllum Miq.: A rare wild betel
Ratnam VK, et al.
International Journal of Pharmacognosy and Phytochemical Research , 7(1), 68-71 (2015)
Phytochemical composition of the essential oils from three Apiaceae species and their antibacterial effects on food-borne pathogens
Oroojalian F, et al.
Food Chemistry, 120(3), 765-770 (2010)
Determination of fragrance ingredients in fish by ultrasound-assisted extraction followed by purge & trap
Chen LC, et al.
Analytical Methods : Advancing Methods and Applications, 9(15), 2237-2245 (2017)
Ion exchange resins as catalyst for the isomerization of ?-pinene to camphene
Chimal-Valencia.O, et al.
BioTechnology: An Indian Journal, 93, 119-123 (2004)
Dendritic growth kinetics and structure II. Camphene
Rubinstein.RE and Glicksman.EM
Journal of Crystal Growth, 112, 97-110 (1991)

Protocolos

Fast GC analysis of sweet orange essential oil in hexane. Key components identified includes: β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

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