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Key Documents

442505

Supelco

Camphene

analytical standard

Sinonimo/i:

DL-Camphene

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About This Item

Formula empirica (notazione di Hill):
C10H16
Numero CAS:
Peso molecolare:
136.23
Numero CE:
Numero MDL:
Codice UNSPSC:
12000000
ID PubChem:

Grado

analytical standard

Livello qualitativo

CdA

current certificate can be downloaded

Confezionamento

ampule of 1000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

159-160 °C (lit.)

Punto di fusione

48-52 °C (lit.)

Densità

0.85 g/mL at 25 °C (lit.)

applicazioni

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

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

[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
CRPUJAZIXJMDBK-DTWKUNHWSA-N

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Descrizione generale

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).

Applicazioni

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.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

4.1B - Flammable solid hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

78.8 °F - DIN 51755 Part 1

Punto d’infiammabilità (°C)

26 °C - DIN 51755 Part 1

Dispositivi di protezione individuale

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


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Certificati d'analisi (COA)

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γ-Terpinene 97%

Sigma-Aldrich

223190

γ-Terpinene

(+)-β-Pinene analytical standard

Supelco

80607

(+)-β-Pinene

α-Pinene primary reference standard

00040590

α-Pinene

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.

Protocolli

-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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