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21365

(−)-Camphor-10-sulfonic acid

purum, ≥98.0% (T)

Synonym(s):

(1R)-(−)-Camphor-10-sulfonic acid

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About This Item

Empirical Formula (Hill Notation):
C10H16O4S
CAS Number:
35963-20-3
Molecular Weight:
232.30
UNSPSC Code:
12352115
NACRES:
NA.22
PubChem Substance ID:
329752149
EC Number:
252-817-9
Beilstein/REAXYS Number:
2809676
MDL number:
MFCD00064158

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Product Name

(−)-Camphor-10-sulfonic acid, purum, ≥98.0% (T)

InChI key

MIOPJNTWMNEORI-XVKPBYJWSA-N

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-/m0/s1

SMILES string

CC1(C)C2CC[C@]1(CS(O)(=O)=O)C(=O)C2

grade

purum

assay

≥98.0% (T)

optical activity

[α]20/D −21.5±1°, c = 10% in H2O

functional group

ketone
sulfonic acid

Quality Level

200

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1 of 3

This Item
2136086090
(−)-Camphor-10-sulfonic acid purum, ≥98.0% (T)

Sigma-Aldrich

21365

(−)-Camphor-10-sulfonic acid

(+)-Camphor-10-sulfonic acid purum, ≥98.0% (T)

Sigma-Aldrich

21360

(+)-Camphor-10-sulfonic acid

Sulfanilic acid puriss. p.a., ≥99.0% (T)

Sigma-Aldrich

86090

Sulfanilic acid

assay

≥98.0% (T)

assay

≥98.0% (T)

assay

≥99.0% (T)

Quality Level

200

Quality Level

200

Quality Level

200

grade

purum

grade

purum

grade

puriss. p.a.

optical activity

[α]20/D −21.5±1°, c = 10% in H2O

optical activity

[α]20/D +21.5±1°, c = 10% in H2O

optical activity

-

functional group

ketone

functional group

ketone, sulfonic acid

functional group

sulfonic acid

Disclaimer

may contain some dark particles

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBR1104V

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Ruizhi Pang et al.
Journal of colloid and interface science, 510, 127-132 (2017-09-25)
Thin film nanocomposite reverse osmosis (TFN RO) membranes incorporated with hydrophilic nanoparticles show a potential problem that the salt rejection can not be improved significantly. In this study, novel TFN RO membranes incorporated with hydrophobic fluorinated silica nanoparticles were fabricated
Determination of 10-camphorsulphonates in pharmaceutical formulations by high-performance liquid chromatography.
C Pierron et al.
Journal of chromatography, 511, 367-372 (1990-07-06)
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
Anne-Catherine Servais et al.
Electrophoresis, 25(16), 2701-2710 (2004-09-08)
The enantiomeric separation of a series of basic pharmaceuticals (beta-blockers, local anesthetics, sympathomimetics) has been investigated in nonaqueous capillary electrophoresis (NACE) systems using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin (HDMS-beta-CD) in combination with potassium camphorsulfonate (camphorSO3-). For this purpose, a face-centered central composite design with
Suh-Jen Jane Tsai et al.
Journal of chromatography. A, 1218(3), 524-533 (2010-12-24)
An effective method has been developed for quantitative determination of six bile acids including lithocholic acid (LCA), deoxycholic acid (DCA), chenodeoxycholic acid (CDCA), hydodeoxycholic acid (HDCA), cholic acid (CA) and ursodeoxycholic acid (UDCA) in biological tissues including pig liver, pig
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