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21293

Supelco

(−)-Camphor

analytical standard

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C10H16O
Numéro CAS:
464-48-2
Poids moléculaire :
152.23
Numéro Beilstein :
1907612
Numéro CE :
207-354-7
Numéro MDL:
MFCD00064148
Code UNSPSC :
85151701
ID de substance PubChem :
329752133
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥99.0% (GC)

Activité optique

[α]20/D −43±1°, c = 10% in ethanol

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

food and beverages

Format

neat

Chaîne SMILES 

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

Clé InChI

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.

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Warning

Mentions de danger

H228,H315,H319,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

4.1B - Flammable solid hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

149.0 °F - closed cup

Point d'éclair (°C)

65 °C - closed cup

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL4043
BCCK6679
BCCH5595
BCCD9733
BCBX0173

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

Sigma-Aldrich

20506

(±)-Camphor

(−)-Borneol analytical standard

Supelco

15598

(−)-Borneol

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

Sigma-Aldrich

21310

(±)-Camphor

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
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
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
Camphor: a chiral starting material in natural product synthesis.
T Money
Natural product reports, 2(3), 253-289 (1985-06-01)
Shigeki Yamamoto et al.
Journal of computational chemistry, 34(25), 2152-2158 (2013-07-05)
Induced resonance Raman optical activity (IRROA) proved to be a very sensitive method to detect molecular chirality. It is exhibited, for example, by complexes of lanthanides with chiral alcohols or ketones. So far, the phenomenon has not been understood at
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Chromatograms

suitable for GC

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