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Camphene

analytical standard

Synonyme(s) :

DL-Camphene

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About This Item

Formule empirique (notation de Hill):
C10H16
Numéro CAS:
Poids moléculaire :
136.23
Numéro CE :
Numéro MDL:
Code UNSPSC :
12000000
ID de substance PubChem :

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 1000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

159-160 °C (lit.)

Pf

48-52 °C (lit.)

Densité

0.85 g/mL at 25 °C (lit.)

Application(s)

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

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

[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

Clé InChI

CRPUJAZIXJMDBK-DTWKUNHWSA-N

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Description générale

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.

Pictogrammes

FlameExclamation markEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

4.1B - Flammable solid hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

78.8 °F - DIN 51755 Part 1

Point d'éclair (°C)

26 °C - DIN 51755 Part 1

Équipement de protection individuelle

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


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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)
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)
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)
Dendritic growth kinetics and structure II. Camphene
Rubinstein.RE and Glicksman.EM
Journal of Crystal Growth, 112, 97-110 (1991)
M Tiwari et al.
Toxicology in vitro : an international journal published in association with BIBRA, 23(2), 295-301 (2009-01-13)
Exploration of antioxidants of plant origin and scientific validation of their efficacies has unraveled bioactives from natural sources. In this study, two terpenoids camphene and geraniol were assessed for their cytoprotective and antioxidant potential using t-BHP stressed rat alveolar macrophages.

Protocoles

-Pinocarveol; Menthol; (+)-Terpinen-4-ol; α-Terpineol; (±)-α-Terpinyl acetate, predominantly α-isomer; Germacrene D

Cymene; 4,5,6,7-Tetrahydro-3,6-dimethylbenzofuran; Linalool; Menthol; Menthone; Menthyl acetate; Germacrene D; Bicyclogermacrene; Thymol

-α-Bergamotene; β-Bisabolene; α-Terpineol; Neryl acetate; Geranyl acetate; Neral; Geranial

-3,7-Dimethyl-2,6-octadien-1-ol; Neral; Geraniol; Geranial; Undecanal; Citronellyl acetate; Neryl acetate; 3,7-Dimethyl-2,6-octadienyl acetate; 1-Tetradecene; Tetradecane; α-Bisabolol

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