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50843

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D-Camphor

analytical standard

Synonyme(s) :

2-Bornanone, 2-Camphanone

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About This Item

Formule empirique (notation de Hill):
C10H16O
Numéro CAS:
464-49-3
Poids moléculaire :
152.23
Numéro CE :
207-355-2
Numéro MDL:
MFCD00064149
Code UNSPSC :
85151701
ID de substance PubChem :
329757640
Nomenclature NACRES :
NA.24

Niveau de qualité

100

Qualité

analytical standard

Densité de vapeur

5.24 (vs air)

Pression de vapeur

4 mmHg ( 70 °C)

Pureté

≥97.5% (GC)

Activité optique

[α]/D +43.0±2.0°, c = 10 in ethanol

Température d'inflammation spontanée

870 °F

Durée de conservation

limited shelf life, expiry date on the label

Limite d'explosivité

3.5 %

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

178-182 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

CC1(C)[C@@H]2CC[C@@]1(C)C(=O)C2

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

D-Camphor is an acyclic terpenoid, that occurs naturally in the wood of Cinnamomum camphora.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Mention d'avertissement

Danger

Mentions de danger

H228,H315,H318,H332,H371

Classification des risques

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

Organes cibles

Lungs

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)

147.2 °F - closed cup

Point d'éclair (°C)

64 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
BCCD4182
BCBW7131
BCBQ7460V
BCBK8372V
BCBK8372

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(±)-Camphor purum, synthetic, ≥95.0% (GC)

Sigma-Aldrich

21310

(±)-Camphor

Camphor 96%

Sigma-Aldrich

148075

Camphor

(±)-Camphor ≥95.5%

Sigma-Aldrich

W526606

(±)-Camphor

The Pharmacology of Chinese Herbs, Second Edition (1998)
R E White et al.
Archives of biochemistry and biophysics, 228(2), 493-502 (1984-02-01)
Three alicyclic compounds (D-camphor, adamantanone, adamantane) were found to be hydroxylated by the cytochrome P-450 isoenzymes P-450cam and P-450LM2. With P-450cam as the catalyst only one product was formed from each of the substrates: 5-exohydroxycamphor, 5-hydroxyadamantanone, and 1-adamantanol. With P-450LM2
D E Gibson et al.
The American journal of emergency medicine, 7(1), 41-43 (1989-01-01)
Camphor ingestion is a toxic ingestion that is seen infrequently in the emergency department. It is remarkable for its rapidity of action and toxicity. A case of camphor ingestion that displayed toxic effects is presented. The pharmacology, manifestations, and management
Equilibrium states and dynamic reactions of iron in the camphor monoxygenase system.
I C Gunsalus et al.
Advances in experimental medicine and biology, 74, 254-262 (1976-01-01)
E Siegel et al.
Pediatric clinics of North America, 33(2), 375-379 (1986-04-01)
Camphor is present in several over-the-counter compounds of questionable use and therefore may be ingested by small children. Because seizures may follow ingestion of certain amounts, appropriate treatment is needed, including the use of anticonvulsants.
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