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21293

Supelco

(−)-Camphor

analytical standard

Sinónimos:

(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

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About This Item

Fórmula empírica (notación de Hill):
C10H16O
Número de CAS:
464-48-2
Peso molecular:
152.23
Beilstein/REAXYS Number:
1907612
EC Number:
207-354-7
MDL number:
MFCD00064148
UNSPSC Code:
85151701
PubChem Substance ID:
329752133
NACRES:
NA.24

grade

analytical standard

Quality Level

100

assay

≥99.0% (GC)

optical activity

[α]20/D −43±1°, c = 10% in ethanol

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

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

InChI key

DSSYKIVIOFKYAU-OIBJUYFYSA-N

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Application

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

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 1

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCL4043
BCCK6679
BCCH5595
BCCD9733
BCBX0173

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

Sigma-Aldrich

20506

(±)-Alcanfor

(−)-Borneol analytical standard

Supelco

15598

(−)-Borneol

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

Sigma-Aldrich

21310

(±)-Alcanfor

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
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
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
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Chromatograms

suitable for GC

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