21370
(±)-Campher-10-sulfonsäure
purum, ≥98.0% (T)
Synonym(e):
(±)-β-Camphorsulfonsäure
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Empirische Formel (Hill-System):
C10H16O4S
CAS-Nummer:
Molekulargewicht:
232.30
EC Number:
227-527-0
UNSPSC Code:
12352106
PubChem Substance ID:
Beilstein/REAXYS Number:
3205973
MDL number:
Technischer Dienst
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Unterstützung erhaltengrade
purum
assay
≥98.0% (T)
form
solid
impurities
≤1% water
mp
199-201 °C (dec.)
SMILES string
CC1(C)[C@@H]2CC[C@@]1(CS(O)(=O)=O)C(=O)C2
InChI
1S/C10H16O4S/c1-9(2)7-3-4-10(9,8(11)5-7)6-15(12,13)14/h7H,3-6H2,1-2H3,(H,12,13,14)/t7-,10-/m1/s1
InChI key
MIOPJNTWMNEORI-GMSGAONNSA-N
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Lagerklasse
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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[D-camphor-beta-sulfonic acid as an ion-pair reagent for the determination of biogenic amines and their metabolites in the rat brain by reverse phase high performance liquid chromatography].
X R Xu et al.
Zhongguo yao li xue bao = Acta pharmacologica Sinica, 8(2), 113-117 (1987-03-01)
Kaoru Nobuoka et al.
Physical chemistry chemical physics : PCCP, 9(44), 5891-5896 (2007-11-09)
We directly observe the interaction between 1-butyl-3-methylimidazolium (bmim) or 1-butyl-2,3-dimethylimidazolium (bm(2)im) and the solute, ethyl acrylate (EA), which is the popular dienophile in the Diels-Alder reaction and an H-bonding acceptor, by using specially designed electrospray mass spectrometry. In imidazolium ionic
Per J Garegg et al.
Carbohydrate research, 337(6), 517-521 (2002-03-14)
The transglucosidations of methyl 4-O-methyl-alpha- and -beta-D-glucopyranoside in ethanolic camphor-10-sulfonic acid, and of ethyl 4-O-methyl-alpha- and -beta-D-glucopyranoside in methanolic camphor-10-sulfonic acid, have been studied. Samples were removed at intervals and the proportions of the glucosides determined by GC of their