C0405000

Camphor (racemic)

Name: Camphor (racemic)
Brand: SIAL
Price: 973 PLN

European Pharmacopoeia (EP) Reference Standard

Synonim(y):

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

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50 MG

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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):

C₁₀H₁₆O

Numer CAS:

76-22-2

Masa cząsteczkowa:

152.23

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329774783

MDL number:

MFCD00074738

Beilstein/REAXYS Number:

1907611

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Nazwa produktu

Camphor (racemic), European Pharmacopoeia (EP) Reference Standard

InChI key

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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

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

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Pharmacopeia & Metrological Institute Standards

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Ta pozycja	02070595	20506	148075
C0405000 Camphor (racemic)	02070595 Kamfora (dl)	Sigma-Aldrich 20506 (±)-Camphor	Sigma-Aldrich 148075 Kamfora
manufacturer/tradename EDQM	manufacturer/tradename HWI	manufacturer/tradename -	manufacturer/tradename -
grade pharmaceutical primary standard	grade primary reference standard	grade -	grade -
format neat	format -	format -	format -
application(s) pharmaceutical (small molecule)	application(s) cleaning products cosmetics flavors and fragrances food and beverages personal care	application(s) pharmaceutical (small molecule)	application(s) -
vapor density 5.2 (vs air)	vapor density 5.2 (vs air)	vapor density 5.2 (vs air)	vapor density 5.2 (vs air)
vapor pressure 4 mmHg ( 70 °C)	vapor pressure 4 mmHg ( 70 °C)	vapor pressure 4 mmHg ( 70 °C)	vapor pressure 4 mmHg ( 70 °C)

Application

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

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.

Other Notes

Sales restrictions may apply.

Packaging

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

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Opis

Cennik

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PHR2427

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PHR2429

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PHR2430

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

PHR2425

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

PHR2431

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

PHR2426

Camphor Impurity B, Camphene, pharmaceutical secondary standard, certified reference material

PHR2805

Methyl Benzylidene Camphor, Pharmaceutical Secondary Standard; Certified Reference Material

pictograms

GHS02,GHS08,GHS05,GHS07,GHS09

signalword

Danger

hcodes

H228,H315,H318,H332,H371,H411

pcodes

P210 - P273 - P280 - P304 + P340 + P312 - P305 + P351 + P338 - P308 + P311

Hazard Classifications

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

Klasa składowania

4.1B - Flammable solid hazardous materials

wgk

WGK 1

flash_point_f

147.9 °F - closed cup

flash_point_c

64.4 °C - closed cup

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Odwiedź Bibliotekę dokumentów

Induction of DNA double-strand breaks by monochlorophenol isomers and ChKM in human gingival fibroblasts.

M Shehata et al.

Archives of toxicology, 86(9), 1423-1429 (2012-05-23)

Phenol has been traditionally used in dental treatment as a sedative for the pulp or as disinfectant for carious cavity and root canal. However, phenol is regarded as a mutagenic and carcinogenic agent and its use in dental practice is

Simultaneous resonance Raman optical activity involving two electronic states.

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

Spontaneous motion of an elliptic camphor particle.

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

Chiroptical spectra of tetrakis (+)-3-heptafluorobutylrylcamphorate Ln(III) complexes with an encapsulated alkali metal ion: solution structures as revealed by chiroptical spectra.

Dai Shirotani et al.

Chirality, 24(12), 1055-1062 (2012-09-05)

The preparation of tetrakis((+)-hfbc) lanthanide(III) complexes with an encapsulated alkali metal and ammonium ions M[Ln((+)-hfbc)(4)] (hereafter abbreviated as M-Ln : (+)-hfbc, (+)-heptafluorobutyrylcamphorate; M, ammonium or benzyl ammonium ions as well as alkali metal ions) was reported and discussed. The electronic circular dichroism

The use of deuterated camphor as a substrate in (1)H ENDOR studies of hydroxylation by cryoreduced oxy P450cam provides new evidence of the involvement of compound I.

Roman Davydov et al.

Biochemistry, 52(4), 667-671 (2012-12-12)

Electron paramagnetic resonance and (1)H electron nuclear double resonance (ENDOR) spectroscopies have been used to analyze intermediate states formed during the hydroxylation of (1R)-camphor (H(2)-camphor) and (1R)-5,5-dideuterocamphor (D(2)-camphor) as induced by cryoreduction (77 K) and annealing of the ternary ferrous

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