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(1S)-(−)-Camphanic chloride

for chiral derivatization, LiChropur, ≥98.0%

Synonym(s):

(−)-Camphanoyl chloride, (1S)-3-Oxo-4,7,7-trimethyl-2-oxabicyclo[2.2.1]heptane-1-carbonyl chloride

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About This Item

Linear Formula:
C10H13O3Cl
CAS Number:
Molecular Weight:
216.66
Beilstein:
3590860
EC Number:
MDL number:
UNSPSC Code:
23151817
PubChem Substance ID:
NACRES:
NA.22

grade

for chiral derivatization

Quality Level

product line

ChiraSelect

Assay

≥98.0% (AT)
≥98.0%

form

solid

optical activity

[α]20/D −18±1°, c = 2% in carbon tetrachloride

optical purity

enantiomeric ratio: ≥99.5:0.5 (GC)

quality

LiChropur

technique(s)

HPLC: suitable

mp

67-70 °C
71-73 °C (lit.)

storage temp.

−20°C

SMILES string

CC1(C)[C@@]2(C)CC[C@@]1(OC2=O)C(Cl)=O

InChI

1S/C10H13ClO3/c1-8(2)9(3)4-5-10(8,6(11)12)14-7(9)13/h4-5H2,1-3H3/t9-,10+/m0/s1

InChI key

PAXWODJTHKJQDZ-VHSXEESVSA-N

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General description

(1S)-(-)-Camphanic chloride is a derivatizing agent.

Application

(1S)-(-)-Camphanic chloride may be used in esterification of enantiomers in volatiles releasedf from wheat, in order to determine the proportion of enantiomers and also in quantifying the esters.

Other Notes

Chiral derivatizing reagent used for the determination of enantiomeric purity of alcohols and amines by HPLC

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Legal Information

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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H. Gerlach
Helvetica Chimica Acta, 68, 1815-1815 (1985)
K.D. Ward et al.
Journal of Chromatography A, 478, 169-169 (1989)
Activity of enantiomers of sulcatol on apterae of Rhopalosiphum padi.
Quiroz, A., and H. M. Niemeyer.
Journal of Chemical Ecology, 24, 361-370 (1998)
J.D. Fourneron et al
The Journal of Organic Chemistry, 54, 4686-4686 (1989)
A. Haag et al.
Helvetica Chimica Acta, 63, 10-10 (1980)

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