(1S)-(+)-Camphor-10-sulphonic acid

(1S)-(+)-Camphor-10-sulphonic acid Basic information
Synthesis
Product Name:(1S)-(+)-Camphor-10-sulphonic acid
Synonyms:D-CAMPHORSULFONIC ACID;D(-)-CAMPHORSULPHONIC ACID;D-REYCHLER’S ACID;D-OXO-10-BORNANESULFONIC ACID;(+)-BETA-CAMPHORSULFONIC ACID;(+)-CAMPHOR-10-SULFONIC ACID;(+)-CAMPHOR-10-SULFONIC ACID (BETA);(1S)-(+)-CAMPHOR-10-SULFONIC ACID
CAS:3144-16-9
MF:C10H16O4S
MW:232.3
EINECS:221-554-1
Product Categories:chiral;Pharmaceutical Intermediates;FINE Chemical & INTERMEDIATES;Chiral Compounds;Bicyclic Monoterpenes;Biochemistry;for Resolution of Bases;Optical Resolution;Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Terpenes;Peptide;Sulfur & Selenium Compounds;3144-16-9;3597-91-9
Mol File:3144-16-9.mol
(1S)-(+)-Camphor-10-sulphonic acid Structure
(1S)-(+)-Camphor-10-sulphonic acid Chemical Properties
Melting point 196-200 °C (dec.)(lit.)
alpha 22 º (589nm, c=20, H2O 25 ºC)
Boiling point 344.46°C (rough estimate)
density 1.2981 (rough estimate)
refractive index 21.5 ° (C=5, H2O)
storage temp. Store below +30°C.
solubility Exhibit moderate solubility in HCCl.
pka1.17±0.50(Predicted)
form Crystalline Powder
color White to off-white
PH0.3 (200g/l, H2O)
optical activity[α]20/D +21.5±1°, c = 10% in H2O
Water Solubility SOLUBLE
Sensitive Hygroscopic
Merck 14,1734
BRN 2809675
Stability:Stable. Protect from moisture. Incompatible with strong oxidizing agents, strong bases.
InChIKeyMIOPJNTWMNEORI-GMSGAONNSA-N
CAS DataBase Reference3144-16-9(CAS DataBase Reference)
EPA Substance Registry SystemBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S,4R)- (3144-16-9)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45-25-27
RIDADR UN 3261 8/PG 2
WGK Germany 3
RTECS ED1550000
3-10
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29147090
MSDS Information
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1S-(+)-Camphor-10-sulfonic acidEnglish
SigmaAldrichEnglish
ACROSEnglish
ALFAEnglish
(1S)-(+)-Camphor-10-sulphonic acid Usage And Synthesis
Synthesis(1S)-(+)-Camphor-10-sulphonic acid can be obtained from natural camphor by brominated sulfonation .
Chemical Propertieswhite to light beige powder
Uses(1S)-(+)-Camphor-10-sulfonic acid is used as stabilizer. (+)-(1S)-camphor-10-sulfonic acid being a very effective resolving agent. . Chiral polyaniline(PANI) nanofibers were synthesized via facilely potentiostatic electropolymerization method without template in the presence of(1S)-(+)camphor-10-sulfonic acid(D-CSA) or(1R)-(-)camphor-10-sulfonic acid(L-CSA) as the dopant. Synthesis of QUATs derived from (1S)-(+)camphor-10-sulfonic acid.
UsesUsed as a resolving agent, and as a catalyst for coupling dipeptides.
DefinitionChEBI: (S)-camphorsulfonic acid is the S enantiomer of camphorsulfonic acid. It is a conjugate acid of a (S)-camphorsulfonate. It is an enantiomer of a (R)-camphorsulfonic acid.
Purification MethodsCrystallise the acid from ethyl acetate and dry it under vacuum (deliquescent). [Loudon J Chem Soc 823 1933, Komppa J Prakt Chem 162 19 1943, Beilstein 11 IV 642.] See above for RS-isomer.
(1S)-(+)-Camphor-10-sulphonic acid Preparation Products And Raw materials
Preparation Products(S)-(+)-3-Quinuclidinol–>Levamisole hydrochloride–>Seratrodast–>7-HYDROXYFLAVANONE–>(1S)-(-)-3-OXOCAMPHORSULFONYLIMINE 98+%

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