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Details

Stereochemistry RACEMIC
Molecular Formula C10H16O4S
Molecular Weight 232.297
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPHORSULFONIC ACID, (±)-

SMILES

CC1(C)[C@@H]2CC[C@@]1(CS(O)(=O)=O)C(=O)C2

InChI

InChIKey=MIOPJNTWMNEORI-GMSGAONNSA-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-/m1/s1

HIDE SMILES / InChI

Approval Year

Unknown
149124
Name Type Language
CAMPHORSULFONIC ACID, (±)-
Common Name English
ECAMSULE RELATED COMPOUND D
USP   USP-RS  
Preferred Name English
ECAMSULE RELATED COMPOUND D [USP IMPURITY]
Common Name English
ECAMSULE RELATED COMPOUND D [USP-RS]
Common Name English
(±)-CAMPHOR-10-SULFONIC ACID
Common Name English
CAMPHOR-10-SULFONIC ACID
Common Name English
VORICONAZOLE RELATED COMPOUND F [USP-RS]
Common Name English
VORICONAZOLE IMPURITY E [EP IMPURITY]
Common Name English
(RS)-10-CAMPHORSULFONIC ACID
Common Name English
2-OXO-10-BORNANESULFONIC ACID
Common Name English
(±)-CAMPHORSULFONIC ACID
Common Name English
BICYCLO(2.2.1)HEPTANE-1-METHANESULFONIC ACID, 7,7-DIMETHYL-2-OXO-
Systematic Name English
(1SR,4RS)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid
Systematic Name English
DL-CAMPHORSULFONIC ACID
Common Name English
ECAMSULE RELATED COMPOUND D RS
Common Name English
Camphorsulfonic acid [WHO-DD]
Common Name English
VORICONAZOLE RELATED COMPOUND F
USP   USP-RS  
Common Name English
VORICONAZOLE RELATED COMPOUND F [USP IMPURITY]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
227-527-0
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-949-2
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
ALTERNATIVE
EPA CompTox
DTXSID60863113
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
SMS_ID
100000153547
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
CAS
76-26-6
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
SUPERSEDED
RS_ITEM_NUM
1231648
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
CAS
5872-08-2
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
FDA UNII
D8D049375Q
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
PRIMARY
RS_ITEM_NUM
1718063
Created by admin on Mon Mar 31 21:32:04 GMT 2025 , Edited by admin on Mon Mar 31 21:32:04 GMT 2025
ALTERNATIVE
NIH
NCATS
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