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02070595

Camphor (dl)

primary reference standard

Synonym(s):

(±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

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100 MG

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
76-22-2
Molecular Weight:
152.23
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329747385
EC Number:
200-945-0
Beilstein/REAXYS Number:
1907611
MDL number:
MFCD00074738

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Product Name

Camphor (dl), primary reference standard

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

grade

primary reference standard

vapor density

5.2 (vs air)

vapor pressure

4 mmHg ( 70 °C)

shelf life

limited shelf life, expiry date on the label

expl. lim.

3.5 %

manufacturer/tradename

HWI

bp

204 °C (lit.)

mp

175-177 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

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1 of 4

This Item
8.4145620506W526606
Camphor (dl) primary reference standard

02070595

Camphor (dl)

DL-Camphor for synthesis

Sigma-Aldrich

8.41456

DL-Camphor

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

Sigma-Aldrich

20506

(±)-Camphor

(±)-Camphor ≥95.5%

Sigma-Aldrich

W526606

(±)-Camphor

grade

primary reference standard

grade

-

grade

-

grade

Fragrance grade, Kosher

vapor density

5.2 (vs air)

vapor density

-

vapor density

5.2 (vs air)

vapor density

5.2 (vs air)

vapor pressure

4 mmHg ( 70 °C)

vapor pressure

1.2 hPa ( 20 °C)

vapor pressure

4 mmHg ( 70 °C)

vapor pressure

4 mmHg ( 70 °C)

shelf life

limited shelf life, expiry date on the label

shelf life

-

shelf life

-

shelf life

-

expl. lim.

3.5 %

expl. lim.

0.6-4.5 % (v/v)

expl. lim.

3.5 %

expl. lim.

3.5 %

manufacturer/tradename

HWI

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

-

Application

Reference Standard in the analysis of herbal medicinal products

General description

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Hazard Classifications

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

signalword

Danger

Storage Class

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

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Certificates of Analysis (COA)

Lot/Batch Number
HWI00167-5
HWI00167-4
HWI00167-3
HWI00167-2
HWI00167

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M Shehata et al.
Archives of toxicology, 86(9), 1423-1429 (2012-05-23)
Phenol has been traditionally used in dental treatment as a sedative for the pulp or as disinfectant for carious cavity and root canal. However, phenol is regarded as a mutagenic and carcinogenic agent and its use in dental practice is
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
Hiroyuki Kitahata et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 87(1), 010901-010901 (2013-02-16)
The coupling between deformation and motion in a self-propelled system has attracted broader interest. In the present study, we consider an elliptic camphor particle for investigating the effect of particle shape on spontaneous motion. It is concluded that the symmetric
Yiji Lin et al.
Dalton transactions (Cambridge, England : 2003), 41(22), 6696-6706 (2012-04-28)
Chiral tetrakis(β-diketonate) Ln(III) complexes Δ-[NaLa(d-hfc)(4)(CH(3)CN)] (1) and Λ-[NaLa(l-hfc)(4) (CH(3)CN)] (2) (d/l-hfc(-) = 3-heptafluo-robutylryl-(+)/(-)-camphorate) are a pair of enantiomers and crystallize in the same Sohncke space group (P2(1)2(1)2(1)) with dodecahedral (DD) geometry. Typically positive and negative exciton splitting patterns around 320
Dahmane El Montassir et al.
Journal of separation science, 36(5), 832-839 (2013-02-05)
In a first step, 26 chiral stationary phases (CSPs) have been screened for the separation of (-)-α-thujone, (+)-β-thujone epimers and camphor enantiomers by LC. The separations were monitored by a polarimeter detector. None of these CSPs provided a noticeable resolution
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