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Safety Information

20506

Sigma-Aldrich

(±)-Camphor

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

Synonym(s):

1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
Molecular Weight:
152.23
Beilstein:
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

Camphor is a crystalline ketone obtained from Cinnamomum Camphora. Its effect on sex hormone has been studied. The camphor derivatives are antiinfluenza compounds that are active against influenza viruses resistant to adamantane-based drugs.

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

20506-4X2KG:
20506-25KG:
20506-2.5KG:
20506-1KG:4548173925851
20506-6X500G:
20506-BULK:
20506-500G:4548173958491
20506-6X1KG:
20506-6X2.5KG:
20506-VAR:
20506-2KG:4548173958484
20506-BULK-RAW:


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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
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
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
Planer nano-graphenes from camphor by CVD.
Somani PR, et al.
Chemical Physics Letters, 430(1), 56-59 (2006)

Protocols

-3,7-Dimethyl-2,6-octadien-1-ol; Neral; Geraniol; Geranial; Undecanal; Citronellyl acetate; Neryl acetate; 3,7-Dimethyl-2,6-octadienyl acetate; 1-Tetradecene; Tetradecane; α-Bisabolol

Chromatograms

suitable for GC

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