Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H8N3O2S2.Na |
| Molecular Weight | 253.277 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].NC(=S)[N-]S(=O)(=O)C1=CC=C(N)C=C1
InChI
InChIKey=AMLYLOFLVJXROT-UHFFFAOYSA-M
InChI=1S/C7H9N3O2S2.Na/c8-5-1-3-6(4-2-5)14(11,12)10-7(9)13;/h1-4H,8H2,(H3,9,10,13);/q;+1/p-1
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C7H9N3O2S2 |
| Molecular Weight | 231.295 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Sample Use Guides
Tests of capacity to inhibit growth showed sulphathiourea to be inferior to sulphadimetine for most Gram-negative organisms except Shigella, but superior to it in its action on Gram-positive organisms, notably haemolytic streptococci and staphylococci. Sulphathiourea is bactericidal when added to a culture in the early stages of growth
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:24:25 GMT 2025
by
admin
on
Mon Mar 31 23:24:25 GMT 2025
|
| Record UNII |
2EA3FMR9NH
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| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
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6101-34-4
Created by
admin on Mon Mar 31 23:24:25 GMT 2025 , Edited by admin on Mon Mar 31 23:24:25 GMT 2025
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m10345
Created by
admin on Mon Mar 31 23:24:25 GMT 2025 , Edited by admin on Mon Mar 31 23:24:25 GMT 2025
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PRIMARY | Merck Index | ||
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2EA3FMR9NH
Created by
admin on Mon Mar 31 23:24:25 GMT 2025 , Edited by admin on Mon Mar 31 23:24:25 GMT 2025
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PRIMARY | |||
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73425401
Created by
admin on Mon Mar 31 23:24:25 GMT 2025 , Edited by admin on Mon Mar 31 23:24:25 GMT 2025
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PRIMARY |