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MilliporeSigma

20506

Sigma-Aldrich

(±)-Alcanfor

meets analytical specification of Ph. Eur., BP, racemic, ≥95% (GC)

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:
Peso molecular:
152.23
Beilstein/REAXYS Number:
1907611
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

5.2 (vs air)

Quality Level

vapor pressure

4 mmHg ( 70 °C)

assay

≥95% (GC)

optical activity

[α]20/D +0.15 to -0.15°, c = 10% in ethanol

quality

meets analytical specification of Ph. Eur., BP
racemic

expl. lim.

3.5 %

impurities

acidity or alcalinity, complies
related subst., complies (GC)
residual solvents, complies
water, complies
≤0.01% halogene compounds (as Cl)
≤0.05% non-volatile matter

bp

204 °C (lit.)

mp

172-180 °C
175-177 °C (lit.)

solubility

carbon disulfide: freely soluble
hexane: freely soluble
liquid sulfur dioxide: soluble
phenol/1,2-dichlorobenzene: soluble

suitability

complies for appearance of solution
passes test for identity

application(s)

pharmaceutical (small molecule)

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

El alcanfor es una cetona cristalina obtenida de Cinnamomum Camphora. Se ha estudiado su efecto sobre las hormonas sexuales. Los derivados del alcanfor son compuestos antigripales activos contra los virus de la gripe resistentes a los medicamentos a base de adamantano.

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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

ppe

dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Los clientes también vieron

New method of preparing high-porosity rapidly saliva soluble compressed tablets using mannitol with camphor, a subliming material.
Koizumi K-I, et al.
International Journal of Pharmaceutics, 152(1), 127-131 (1997)
Anastasiya S Sokolova et al.
Bioorganic & medicinal chemistry, 22(7), 2141-2148 (2014-03-19)
Influenza is a continuing world-wide public health problem that causes significant morbidity and mortality during seasonal epidemics and sporadic pandemics. The purpose of the study was synthesis and investigation of antiviral activity of camphor-based symmetric diimines and diamines. A set
Microbiological degradation of (+)-camphor.
Bradshaw WH, et al.
Journal of the American Chemical Society, 81(20), 5507-5507 (1959)
Sima Shahabi et al.
Cell journal, 16(2), 231-234 (2014-02-26)
In some traditional therapies, it has been claimed that camphor (a crystalline ketone obtained from cinnamomum camphora) would be a suppressor of sexual behaviors and sex hormones. This study evaluated the effects of camphor on sex hormones, like luteinizing hormone
Jan C Schöneboom et al.
Journal of the American Chemical Society, 126(12), 4017-4034 (2004-03-25)
The stereospecific cytochrome P450-catalyzed hydroxylation of the C(5)-H((5-exo)) bond in camphor has been studied theoretically by a combined quantum mechanical/molecular mechanical (QM/MM) approach. Density functional theory is employed to treat the electronic structure of the active site (40-100 atoms), while

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