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21310

Sigma-Aldrich

(±)-Camphor

purum, synthetic, ≥95.0% (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:
76-22-2
Molecular Weight:
152.23
Beilstein:
1907611
EC Number:
200-945-0
MDL number:
MFCD00074738
UNSPSC Code:
12352100
PubChem Substance ID:
329752137
NACRES:
NA.22

vapor density

5.2 (vs air)

Quality Level

200

vapor pressure

4 mmHg ( 70 °C)

grade

purum

Assay

≥95.0% (GC)

quality

synthetic

expl. lim.

3.5 %

impurities

≤0.5% water

bp

204 °C (lit.)

mp

175-177 °C (lit.)

solubility

ethanol: soluble 1 g/10 mL, clear, colorless
water: soluble

functional group

ketone

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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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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL1283
STBK8466
STBK7072
STBK5200
STBK0680

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Planer nano-graphenes from camphor by CVD.
Somani PR, et al.
Chemical Physics Letters, 430(1), 56-59 (2006)
Highly diastereoselective synthesis of new optically active aminoalcohols in one step from (+)-camphor and (-)-fenchone.
Genov M, et al.
Tetrahedron Asymmetry, 8(11), 1869-1876 (1997)
Tamera J Corte et al.
American journal of respiratory and critical care medicine, 190(2), 208-217 (2014-06-18)
Pulmonary hypertension (PH) associated with fibrotic idiopathic interstitial pneumonia (IIP; idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia) confers important additional morbidity and mortality. To evaluate the safety and clinical efficacy of the dual endothelin-1 receptor antagonist bosentan in this patient
Marcello Trevisani et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(33), 13519-13524 (2007-08-09)
TRPA1 is an excitatory ion channel expressed by a subpopulation of primary afferent somatosensory neurons that contain substance P and calcitonin gene-related peptide. Environmental irritants such as mustard oil, allicin, and acrolein activate TRPA1, causing acute pain, neuropeptide release, and
Haoxing Xu et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 25(39), 8924-8937 (2005-09-30)
Camphor is a naturally occurring compound that is used as a major active ingredient of balms and liniments supplied as topical analgesics. Despite its long history of common medical use, the underlying molecular mechanism of camphor action is not understood.
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Chromatograms

suitable for GC

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