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C0405000

Camphor (racemic)

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

(±)-Camphor, 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:
76-22-2
Poids moléculaire :
152.23
Numéro Beilstein :
1907611
Numéro MDL:
MFCD00074738
Code UNSPSC :
41116107
ID de substance PubChem :
329774783
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Densité de vapeur

5.2 (vs air)

Pression de vapeur

4 mmHg ( 70 °C)

Famille d'API

camphor

Limite d'explosivité

3.5 %

Fabricant/nom de marque

EDQM

Point d'ébullition

204 °C (lit.)

Pf

175-177 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

[H][C@](CC1=O)(CC2)C(C)(C)[C@]12C

InChI

1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1

Clé InChI

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Camphor (racemic) EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Conditionnement

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

1087520

D-Camphor sulfonic acid, United States Pharmacopeia (USP) Reference Standard

PHR2427

D-Camphor Impurity A, a-pinene, certified reference material, pharmaceutical secondary standard

PHR2429

(−)-Borneol, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2430

(+)-Fenchol, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2425

(−)-Fenchone, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2431

D-Camphor Impurity I, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2426

Camphene, pharmaceutical secondary standard, certified reference material

PHR2805

Methyl Benzylidene Camphor, Pharmaceutical Secondary Standard; Certified Reference Material

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 2 Inhalation

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)

147.9 °F - closed cup

Point d'éclair (°C)

64.4 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number

Désolés, nous n'avons pas de COA pour ce produit disponible en ligne pour le moment.

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D-Camphor analytical standard

Supelco

50843

D-Camphor

(1R)-(+)-Camphor 98%

Sigma-Aldrich

857300

(1R)-(+)-Camphor

Menthol European Pharmacopoeia (EP) Reference Standard

M0350000

Menthol

Methyl salicylate Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1214

Methyl salicylate

(−)-Menthol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1116

(−)-Menthol

D-Camphor ≥97%, FG

Sigma-Aldrich

W223018

D-Camphor

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
Skrollan Stockinger et al.
Journal of chromatography. A, 1269, 346-351 (2012-08-23)
Novel 3-(perfluoroalkanoyl)-(1R)-camphorate nickel complexes immobilized to poly(dimethylsiloxane) phases are presented. Immobilized 3-(perfluoroalkanoyl)-(1R)-camphorate nickel complexes with a trifluoromethyl (CF(3); nickel(II)-bis[(1R,4S)-3-trifluoromethanoyl-10-propylenoxycamphor]-polysiloxane Ni(tfpc)(2)@PS) and a heptafluoropropyl-substituent (C(3)F(7); nickel(II)-bis[(1R,4S)-3-heptafluorobutanoyl-10-propylenoxycamphor]-polysiloxane Ni(hfpc)(2)@PS) were synthesized, characterized and immobilized to polysiloxane. Ni(hfpc)(2)@PS was immobilized with a selector content
I Jiménez-Díaz et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 936, 80-87 (2013-09-06)
UV-filters are widely used in many personal care products and cosmetics. Recent studies indicate that some organic UV-filters can accumulate in biota and act as endocrine disruptors, but there are few studies on the occurrence and fate of these compounds
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
Dong-Bin Dang et al.
Chemical communications (Cambridge, England), 49(22), 2243-2245 (2013-02-12)
A series of 3D homochiral manganese-lanthanide frameworks have been synthesized based on chiral camphoric acid. In the heterometallic features, D-camphoric acids are unprecedentedly embedded in three coordination modes.
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