Skip to Content
Merck
All Photos(1)

Documents

442505

Supelco

Camphene

analytical standard

Synonym(s):

DL-Camphene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H16
CAS Number:
Molecular Weight:
136.23
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

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

Looking for similar products? Visit Product Comparison Guide

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.

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 2

Flash Point(F)

78.8 °F - DIN 51755 Part 1

Flash Point(C)

26 °C - DIN 51755 Part 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

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)
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)
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)

Protocols

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service