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C0405000

Camphor (racemic)

European Pharmacopoeia (EP) Reference Standard

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C10H16O
Numer CAS:
76-22-2
Masa cząsteczkowa:
152.23
Beilstein:
1907611
Numer MDL:
MFCD00074738
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329774783
NACRES:
NA.24

klasa czystości

pharmaceutical primary standard

gęstość pary

5.2 (vs air)

ciśnienie pary

4 mmHg ( 70 °C)

rodzina API

camphor

granice wybuchowości

3.5 %

producent / nazwa handlowa

EDQM

bp

204 °C (lit.)

mp

175-177 °C (lit.)

Zastosowanie

pharmaceutical (small molecule)

Format

neat

ciąg 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

Klucz InChI

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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Opis ogólny

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.

Zastosowanie

Kamfora (racemiczna) EP Wzorzec odniesienia, przeznaczony do stosowania w badaniach laboratoryjnych wyłącznie zgodnie z zaleceniami Farmakopei Europejskiej.

Opakowanie

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

Inne uwagi

Sales restrictions may apply.
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Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

H228,H315,H318,H332,H371,H411

Klasyfikacja zagrożeń

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

Kod klasy składowania

4.1B - Flammable solid hazardous materials

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

147.9 °F - closed cup

Temperatura zapłonu (°C)

64.4 °C - closed cup

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Certyfikaty analizy (CoA)

Lot/Batch Number

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D-Camphor analytical standard

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Sigma-Aldrich

857300

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Menthol European Pharmacopoeia (EP) Reference Standard

M0350000

Menthol

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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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