Key Documents

View All Documentation

21370

(±)-Camphor-10-sulfonic acid

Name: (±)-Camphor-10-sulfonic acid
Brand: SIAL

purum, ≥98.0% (T)

Synonym(s):

(±)-β-Camphorsulfonic acid

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₆O₄S

CAS Number:

5872-08-2

Molecular Weight:

232.30

EC Number:

227-527-0

UNSPSC Code:

12352106

PubChem Substance ID:

329752150

Beilstein/REAXYS Number:

3205973

MDL number:

MFCD00074827

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

grade

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

Description

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

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

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Determination of bile acids in pig liver, pig kidney and bovine liver by gas chromatography-chemical ionization tandem mass spectrometry with total ion chromatograms and extraction ion chromatograms.

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

Transglucosidation of methyl and ethyl D-glucopyranosides by alcoholysis.

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

Enantiomeric separation of basic compounds using heptakis(2,3-di-O-methyl-6-O-sulfo)-beta-cyclodextrin in combination with potassium camphorsulfonate in nonaqueous capillary electrophoresis: optimization by means of an experimental design.

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

View All Related Papers