L-Camphorsulfonic acid Uses Production method
ChemicalBook > CAS DataBase List > (1R)-(-)-10-Camphorsulfonic acid

(1R)-(-)-10-Camphorsulfonic acid

L-Camphorsulfonic acid Uses Production method
Product Name
(1R)-(-)-10-Camphorsulfonic acid
CAS No.
35963-20-3
Chemical Name
(1R)-(-)-10-Camphorsulfonic acid
Synonyms
(-)-CSA;(1R)-(-)-CAMPHOR-10-SULFONIC ACID;((1R,4S)-7,7-DiMethyl-2-oxobicyclo[2.2.1]heptan-1-yl)Methanesulfonic acid;(-)-10-CSA;L-(-)-CAMPHORSULFONIC ACID;(-)-10-CAMPHORSULFONIC ACID;d-Camphor-10-sulphonic acid;(-)-10-Camphorsulfonic Acid;(1R)-CAMPHOR-10-SULFONIC ACID;L-10-(-)-CAMPHOR SULFONIC ACID
CBNumber
CB0365888
Molecular Formula
C10H16O4S
Formula Weight
232.3
MOL File
35963-20-3.mol
More
Less

(1R)-(-)-10-Camphorsulfonic acid Property

Melting point:
198 °C (dec.)(lit.)
alpha 
-22 º (c=20,H2O)
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 
DMSO (Slightly), Methanol (Slightly), Water (Sparingly)
pka
1.17±0.50(Predicted)
form 
Crystalline Powder
color 
White to slightly beige
PH
1.2-1.4 (20g/l, H2O)
optical activity
[α]20/D 21°, c = 2 in H2O
Water Solubility 
soluble
Sensitive 
Hygroscopic
BRN 
2809676
Stability:
Stable. Hygroscopic. Incompatible with strong bases, strong oxidizing agents.
InChIKey
MIOPJNTWMNEORI-XVKPBYJWSA-N
CAS DataBase Reference
35963-20-3(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-36/37/39-45-24/25-27
RIDADR 
UN 3261 8/PG 2
WGK Germany 
3
3-10
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29147090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H314Causes severe skin burns and eye damage

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P363Wash contaminated clothing before reuse.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.40094
Product name
(1R)-(-)-Camphor-10-sulfonic acid
Purity
for synthesis
Packaging
100g
Price
$177
Updated
2024/03/01
Sigma-Aldrich
Product number
21365
Product name
(?)-Camphor-10-sulfonic acid
Purity
purum,≥98.0%(T)
Packaging
50g
Price
$99.5
Updated
2024/03/01
Sigma-Aldrich
Product number
21365
Product name
(?)-Camphor-10-sulfonic acid
Purity
purum,≥98.0%(T)
Packaging
250g
Price
$344
Updated
2024/03/01
TCI Chemical
Product number
C0972
Product name
(-)-10-Camphorsulfonic Acid
Purity
>98.0%(T)
Packaging
25g
Price
$30
Updated
2024/03/01
TCI Chemical
Product number
C0972
Product name
(-)-10-Camphorsulfonic Acid
Purity
>98.0%(T)
Packaging
100g
Price
$71
Updated
2024/03/01
More
Less

(1R)-(-)-10-Camphorsulfonic acid Chemical Properties,Usage,Production

L-Camphorsulfonic acid

Camphor sulfonic acid includes L-camphor sulfonic acid, D-camphor sulfonic acid and racemic camphor sulfonic acid these three isomers.
It is a kind of white columnar crystals with the melting point of 193°C (decomposition). [α]D20+24° (water). It is Slightly soluble in ethanol, insoluble in ether, soluble in sodium hydroxide and sodium carbonate solution. L-camphor sulfonic acid could be produced from reaction between camphor, sulfuric acid and acetic anhydride.It has a lot of functions such as exciting the respiratory center, the vascular movement center and myocardium. Its sodium salt plays pharmaceutical role in medicine.
Camphor sulfonic acid sodium salt is a kind of white crystalline powder. It is odorless and tastes bitter and then sweet. It is easily absorb moisture and easily dissolve in the water and hot ethanol. So it should be shading confined preservation. it can Directly excite the medulla oblongata respiratory center and vascular movement center, and quicken and deepen the breath, rise the blood pressure; it also can directly excite the myocardium and strength the contraction of cardiac muscle as well as could increase the output.
It is applied the treatment of infectious disease, as well as the disease like central inhibition of poisoning caused by respiratory depression, fatigue, high fever, poisoning, heat stroke and other acute heart failure.

Uses

(1) It is also used for the racemization of optical isomers.
(2) It can be applied to the resolution of intermediate or isomer in medicine.
(3) It also could play a role as organic synthesis intermediates and resolving agent.

Production method

Camphor sulfonic acid is obtained from camphor and sulfuric acid by irradiation.
This method involves:
1) Adding the camphor and acetic anhydride to the pot.
2) Mixing it and making it dissolved.
3) Dripping sulfuric acid after cooling. And the reaction should be maintained at 44-45 °C for 48 hours. Then cool it to 6-7 °C.
4) Crystallizing, filtrating, washing with a small amount of acetic acid crystals, and dry it to get camphor sulfonic acid.

Physical properties

(1R)-(-)-10-Camphorsulfonic acid is a kind of prismatic crystals and its melting point is 193-195 ° C (decompose). It is Insoluble in ether and slightly soluble in glacial acetic acid and ethyl acetate. And it is and moisture in wet air.

Uses

(1R)-(-)-Camphor-10-sulfonic acid, is used as a pharamaceutical intermediate and also used as a chiral derivative of Camp. It can also be used as resolving agents for chiral amines and other cations.

Uses

1R)-(-)-10-Camphorsulfonic acid is a chiral derivative of Camphor.It has the following uses:
(1)It is also used for the racemization of optical isomers.
(2) It can be applied to the resolution of intermediate or isomer in medicine.
(3) It also could play a role as organic synthesis intermediates and resolving agent.

Definition

ChEBI: The R enantiomer of camphorsulfonic acid.

General Description

(1R)-(-)-10-Camphorsulfonic acid is an HPLC derivatization reagent for UV/Vis detection. It is mainly employed for the resolution of bases.

Purification Methods

It forms prisms from AcOH or EtOAc, and is deliquescent in moist air. Store it in tightly stoppered bottles. The NH4 salt forms needles from H2O [] D ±20.5o (c 5, H2O). [Burgess & Lowry J Chem Soc 127 279 1925, Marsi et al. J Am Chem Soc [ 78 3063 1956.] The RS-acid recrystallises from AcOH. [60g of (±)-acid in 60mL of AcOH at 105o gave 40g of crystals has m 202-203o [Bartlett & Knox Org Synth 45 12 1965.] [Beilstein 11 IV 642.]

(1R)-(-)-10-Camphorsulfonic acid Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

(1R)-(-)-10-Camphorsulfonic acid Suppliers

Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
ProdList
9171
Advantage
60
Standardpharm Co. Ltd.
Tel
86-714-3992388
Email
overseasales1@yongstandards.com
Country
United States
ProdList
14332
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10404
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Camphor Technologies Inc.
Tel
--
Fax
--
Country
United States
ProdList
148
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Advanced Synthesis S.A.
Tel
--
Fax
--
Country
United States
ProdList
249
Advantage
58
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
Molcan Corporation
Tel
--
Fax
--
Email
info@molcan.com
Country
United States
ProdList
686
Advantage
60
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Precursor Chemicals, Inc.
Tel
--
Fax
--
Email
info@precursorchem.com
Country
United States
ProdList
347
Advantage
51
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
CarboMer, Inc.
Tel
--
Fax
--
Email
sales@carbomer.com
Country
United States
ProdList
4026
Advantage
67
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
Advanced Asymmetrics, Inc.
Tel
--
Fax
--
Email
sales@advancedasymmetrics.com
Country
United States
ProdList
521
Advantage
42
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Chiral Management
Tel
--
Fax
--
Email
sales@chiralmanagement.com
Country
United States
ProdList
1332
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
Chemiplus Corporation
Tel
--
Fax
--
Email
okazaki@chemiplus.com
Country
United States
ProdList
3198
Advantage
38
M/S PANAMIT INTERNATIONAL
Tel
--
Fax
--
Email
sales@jyotichem.com
Country
United States
ProdList
312
Advantage
46
Empire Chemicals
Tel
--
Fax
--
Email
global@empirechemicals.com
Country
United States
ProdList
190
Advantage
38
D-L Chiral Chemicals, LLC
Tel
--
Fax
--
Country
United States
ProdList
977
Advantage
42
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
Amber Synthetics, Amsyn Inc.
Tel
--
Fax
--
Email
mail@amsyn.com
Country
United States
ProdList
194
Advantage
46
Multilab
Tel
--
Fax
--
Email
sales@multilab.biz
Country
United States
ProdList
94
Advantage
58
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
Chontech, Inc.
Tel
--
Fax
--
Email
chontech@yahoo.com
Country
United States
ProdList
1101
Advantage
30
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Fisher Scientific
Tel
--
Fax
--
Email
sales@fishersci.com
Country
United States
ProdList
2337
Advantage
86
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
More
Less

View Lastest Price from (1R)-(-)-10-Camphorsulfonic acid manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
(1R)-(-)-10-Camphorsulfonic acid 35963-20-3
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-22
airuikechemical co., ltd.
Product
l-10-camphorsulfonic acid 35963-20-3
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
99.9%
Supply Ability
200tons
Release date
2024-03-28
Hebei Chuanghai Biotechnology Co,.LTD
Product
CAMPHORSULFONIC ACID 35963-20-3
Price
US $8.00/kg
Min. Order
10kg
Purity
99%
Supply Ability
10000kg
Release date
2024-08-22

35963-20-3, (1R)-(-)-10-Camphorsulfonic acidRelated Search:


  • (-)-CAMPHOR-10-SULPHONIC ACID
  • (-)-CAMPHOR-10-SULFONIC ACID
  • L-10-(-)-CAMPHOR SULFONIC ACID
  • L-(-)-CAMPHORSULFONIC ACID
  • L-(+)-CAMPHOR SULFONIC ACID
  • L(+)-CAMPHORSULPHONIC ACID
  • L-CAMPHORSULPHONIC ACID
  • L-(-)-CAMPHOR-10-SULFONIC ACID
  • (1R)-(-)-CAMPHOR-10-SULPHONIC ACID
  • (1R)-(-)-CAMPHOR-10-SULFONIC ACID
  • (1R)-CAMPHOR-10-SULFONIC ACID
  • (1R)-(-)-CAMPHORSULFONIC ACID
  • (1r)-[7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulphonic acid
  • (1R)-(-)-10-CAMPHORSULFONIC ACID
  • (-)-10-CAMPHORSULFONIC ACID
  • Voriconazole Related Compound 11
  • 2-Oxo-10-bornane-sulfonicacid
  • 7,7-Dimethyl-2-oxobicyclo[2,2,1]heptane-1-methane-sulfonicacid
  • Camphor-sulphonicacid
  • Voriconazole Related CoMpound F
  • (1R)-(-)-10-Camphosulfonic acid
  • L - Campho 10 Sulphonic Acid
  • (1R)-(-)-Camphor-10-sulfonic acid, 98+%
  • CLOPIDOGREL INTERMEDIATES
  • d-Camphor-10-sulphonic acid
  • (1R)-(-)-CAMPHOR-10-SULPHONIC ACID 99%
  • S-(-)-CAMPHORSULFONIC ACID
  • (1R)-(-)-CAMPHER-10-SULFONSURE
  • Voriconazole EP Impurity E (1R)-Isomer
  • )-Camphor-10-sulfonic acid (1R)-Camphor-10-sulfonic acid L(-)-Camphorsulfonic acid
  • (1R)-(-)-Camphor-10-sulfonic acid for synthesis
  • [(1S,4R)-7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl]methanesulfonic acid
  • (1R)-(-)-10-CaMphorsulfonic acid 98%
  • L- caMphor sulfonic acid (L-caMphor sulfonic acid)
  • L(-)-Camphorsulfonic acid 1R-(-)-10-Camphorsulfonic acid
  • (-)-10-CSA
  • [(4R)-7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl]methanesulfonic acid
  • Camphor Impurity 3((1R)-10-Camphorsulfonic Acid)
  • (-)-CamphorsuL
  • (-)-Camphor-10-sulfonic acid, (1R)-(-)-Camphor-10-sulfonic acid, (1R)-Camphor-10-sulfonic acid
  • (-)-(1R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid
  • Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1R,4S)-
  • (1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid
  • (1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1α-methanesulfonic acid
  • [1R,4S,(-)]-2-Oxobornane-10-sulfonic acid
  • [1R,4S,(-)]-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid
  • (1R)-Camphor-10-sulfonic acid L(-)-Camphorsulfonic acid
  • (-)-10-Camphorsulfonic acid ,99%
  • ()-Camphor-10-sulfonic acid,(1R)-()-Camphor-10-sulfonic acid
  • (1R)-()-10-Camphorsulfonic acid,()-Camphor-10-sulfonic acid, (1R)-()-Camphor-10-sulfonic acid, (1R)-Camphor-10-sulfonic acid
  • L(-)-Camphorsulfonic
  • L(-)-Camphorsulfonic acid,98%
  • (1R)-(-)-CAMPHOR-10-SULPHONIC ACIDCaMphorSulfonic Acid
  • L(-)-CaMphorsulfonic acid, 98% 5GR
  • ((1R,4S)-7,7-DiMethyl-2-oxobicyclo[2.2.1]heptan-1-yl)Methanesulfonic acid
  • (R)-()-10-CaMphorsulfonic acid
  • (-)-10-Camphorsulfonic acid, 99%, reagent grade
  • (-)-10-Camphorsulfonic Acid &gt