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21293

Supelco

(−)-Campher

analytical standard

Synonym(e):

(1S)-1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-on

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About This Item

Empirische Formel (Hill-System):
C10H16O
CAS-Nummer:
464-48-2
Molekulargewicht:
152.23
Beilstein:
1907612
EG-Nummer:
207-354-7
MDL-Nummer:
MFCD00064148
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329752133
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥99.0% (GC)

Optische Aktivität

[α]20/D −43±1°, c = 10% in ethanol

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

food and beverages

Format

neat

SMILES String

CC1(C)[C@H]2CC[C@]1(C)C(=O)C2

InChI

1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m0/s1

InChIKey

DSSYKIVIOFKYAU-OIBJUYFYSA-N

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Anwendung

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

Anwendung

Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

FlameExclamation mark
GHS02,GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

4.1B - Flammable solid hazardous materials

WGK

WGK 1

Flammpunkt (°F)

149.0 °F - closed cup

Flammpunkt (°C)

65 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCL4043
BCCK6679
BCCH5595
BCCD9733
BCBX0173

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(±)-Campher meets analytical specification of Ph. Eur., BP, ≥95% (GC), racemic

Sigma-Aldrich

20506

(±)-Campher

(−)-Borneol analytical standard

Supelco

15598

(−)-Borneol

(±)-Campher purum, synthetic, ≥95.0% (GC)

Sigma-Aldrich

21310

(±)-Campher

Isoborneol analytical standard

Supelco

79856

Isoborneol

DL-Camphor for synthesis

Sigma-Aldrich

8.41456

DL-Camphor

Jeffrey N Love et al.
The Journal of emergency medicine, 27(1), 49-54 (2004-06-29)
Serious pediatric toxicity resulting from exposure to small amounts of camphor-containing products has long been a problem. Twenty years ago the United States Food and Drug Administration took several actions in an attempt to ameliorate this risk. Despite these changes
Yali V Zhang et al.
Nature neuroscience, 16(10), 1468-1476 (2013-09-10)
Animals tend to reject bitter foods. However, long-term exposure to some unpalatable tastants increases acceptance of these foods. Here we show that dietary exposure to an unappealing but safe additive, camphor, caused the fruit fly Drosophila melanogaster to decrease camphor
Hiroyuki Yamashita et al.
Pharmaceutical research, 30(1), 70-80 (2012-08-22)
Although a number of studies have reported that cocrystals can form by heating a physical mixture of two components, details surrounding heat-induced cocrystal formation remain unclear. Here, we attempted to clarify the thermal behavior of a physical mixture and cocrystal
Hiroyuki Kitahata et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 87(1), 010901-010901 (2013-02-16)
The coupling between deformation and motion in a self-propelled system has attracted broader interest. In the present study, we consider an elliptic camphor particle for investigating the effect of particle shape on spontaneous motion. It is concluded that the symmetric
Christian Merten et al.
The journal of physical chemistry. A, 116(27), 7329-7336 (2012-06-06)
In the present work, the first observation of strong resonance Raman optical activity (RROA) involving more that one resonant electronic state is reported. The chiral transition metal complex bis-(trifluoroacetylcamphorato) copper(II), abbreviated Cu(tfc)(2), exhibits both resonance Raman (RR) and RROA spectra
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Chromatograms

suitable for GC

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