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02070595

Camphor (dl)

primary 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 CE :
200-945-0
Numéro MDL:
MFCD00074738
Code UNSPSC :
85151701
ID de substance PubChem :
329747385
Nomenclature NACRES :
NA.24

Qualité

primary reference standard

Densité de vapeur

5.2 (vs air)

Pression de vapeur

4 mmHg ( 70 °C)

Durée de conservation

limited shelf life, expiry date on the label

Limite d'explosivité

3.5 %

Fabricant/nom de marque

HWI

Point d'ébullition

204 °C (lit.)

Pf

175-177 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

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

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Application

Reference Standard in the analysis of herbal medicinal products

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
HWI00167-4
HWI00167-3
HWI00167-2
HWI00167
HWI00167-1

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Si vous avez besoin d'une version particulière, vous pouvez rechercher un certificat spécifique par le numéro de lot.

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Camphor 96%

Sigma-Aldrich

148075

Camphor

Carnosic Acid Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR2208

Carnosic Acid

Methyl salicylate Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1214

Methyl salicylate

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

Sigma-Aldrich

857300

(1R)-(+)-Camphor

D-Camphor ≥97%, FG

Sigma-Aldrich

W223018

D-Camphor

(+)-Borneol analytical standard

Supelco

68878

(+)-Borneol

(1S)-(−)-Camphor 95%

Sigma-Aldrich

C352

(1S)-(−)-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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