Skip to Content
Merck
All Photos(1)

Documents

21310

Sigma-Aldrich

(±)-Camphor

purum, synthetic, ≥95.0% (GC)

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBL3625
STBL1283
STBK8466
STBK2791
STBK7072

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
Planer nano-graphenes from camphor by CVD.
Somani PR, et al.
Chemical Physics Letters, 430(1), 56-59 (2006)
Christian Merten et al.
The journal of physical chemistry. A, 116(27), 7329-7336 (2012-06-06)
In the present work, the first observation of strong resonance Raman optical activity (RROA) involving more that one resonant electronic state is reported. The chiral transition metal complex bis-(trifluoroacetylcamphorato) copper(II), abbreviated Cu(tfc)(2), exhibits both resonance Raman (RR) and RROA spectra
Shigeki Yamamoto et al.
Journal of computational chemistry, 34(25), 2152-2158 (2013-07-05)
Induced resonance Raman optical activity (IRROA) proved to be a very sensitive method to detect molecular chirality. It is exhibited, for example, by complexes of lanthanides with chiral alcohols or ketones. So far, the phenomenon has not been understood at
Hong Zhang et al.
Analytica chimica acta, 742, 67-73 (2012-08-14)
A simple, sensitive and selective method for the simultaneous determination of five ultraviolet (UV) filters: benzophenone, octyl salicylate, homosalate, 3-(4-methylbenzylidene) camphor, 2-hydroxy-4-methoxybenzophenone in aqueous samples was developed. The analytes were extracted by plunger-in-needle solid-phase microextraction with graphene as sorbent, then
View All Related Papers

Chromatograms

suitable for GC

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service