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C0405000

(±)-Alcanfor

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

1,7,7-trimetilbiciclo[2,2.1]heptan-2-ona

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About This Item

Fórmula empírica (notación de Hill):
C10H16O
Número de CAS:
76-22-2
Peso molecular:
152.23
Beilstein/REAXYS Number:
1907611
MDL number:
MFCD00074738
UNSPSC Code:
41116107
PubChem Substance ID:
329774783
NACRES:
NA.24

grade

pharmaceutical primary standard

vapor density

5.2 (vs air)

vapor pressure

4 mmHg ( 70 °C)

API family

camphor

expl. lim.

3.5 %

manufacturer/tradename

EDQM

bp

204 °C (lit.)

mp

175-177 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

SMILES string

[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

InChI key

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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General description

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.

Packaging

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

Other Notes

Sales restrictions may apply.

Related product

Referencia del producto
Descripción
Precios

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

signalword

Danger

Hazard Classifications

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

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 1

flash_point_f

147.9 °F - closed cup

flash_point_c

64.4 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number

Lo sentimos, en este momento no disponemos de COAs para este producto en línea.

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Slide 1 of 6

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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

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.
Guofeng Shang et al.
Journal of the Air & Waste Management Association (1995), 62(8), 873-879 (2012-08-25)
The characteristics and mechanisms of hydrogen sulfide (H2S) adsorption on a biochar through pyrolysis at various temperatures (100 to 500 degrees C) were investigated. The biochar used in the current study was derived from the camphor tree (Cinnamomum camphora). The
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
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
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