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Cat. No.: HY-B1236A

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Sulfacarbamide sodium

(Synonyms: Sulfanilylurea sodium; Urosulfan sodium)

2 Cited Publications

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Based on 2 publication(s) in Google Scholar

Sulfacarbamide (Sulfanilylurea, Urosulfan) sodium is a class of sulfonamides with an antimicrobial activity. Sulfacarbamide sodium can be used for the study of diabetes.

For research use only. We do not sell to patients.

CAS No.: 4675-90-5
Formula: C₇H₈N₃NaO₃S
Molecular Weight:237.21

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (268 KB)

Sulfacarbamide sodium Chemical Structure

CAS No.: 4675-90-5

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Biological Activity

Description

Sulfacarbamide (Sulfanilylurea, Urosulfan) sodium is a class of sulfonamides with an antimicrobial activity. Sulfacarbamide sodium can be used for the study of diabetes^[1]^[2].

Chemical Information

CAS No. 4675-90-5
Molecular Weight 237.21
Formula C₇H₈N₃NaO₃S
SMILES

O=S(C1=CC=C(N)C=C1)(/N=C(N)\[O-])=O.[Na+]
Synonyms

Sulfanilylurea sodium; Urosulfan sodium
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Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Publications (2)

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ACS Environ Au

Machine Learning-Assisted Recognition of Environmental Sulfur-Containing Chemicals in Nontargeted Mass Spectrometry Analysis of Inadequate Mass Resolution. [Abstract]

2025 Aug 5;5(6):573-582. PMID: 41277996
Anal Chem

Exposome-Scale Investigation of Cl-/Br-Containing Chemicals Using High-Resolution Mass Spectrometry, Multistage Machine Learning, and Cloud Computing. [Abstract]

2025 Jun 3;97(21):11099-11109. PMID: 40401576

Purity & Documentation

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Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (268 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Dorofeenko, G.N., et al. Antimicrobial and antiviral activity of pyridinium salts. Pharm Chem J 16, 583-586 (1982).

[2]. WILD H, et al. [Clinical observations on injuries to the peripheral nervous system and liver in diabetics receiving sulfanilylurea]. Dtsch Med J. 1959 Jun 5;10(8):286-92. [Content Brief]

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How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

Sulfacarbamide sodium

2 Cited Publications

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Sulfacarbamide sodium

Publications Citing Use of MedChemExpress (MCE) Sulfacarbamide sodium

Biological Activity

Chemical Information

Publications (2)

Purity & Documentation

References

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Sulfacarbamide sodium Related Classifications

HY-B1236A Related Classifications