ChemicalBook >> CAS DataBase List >>Carzenide

Carzenide

CAS No.
138-41-0
Chemical Name:
Carzenide
Synonyms
4-SULFAMOYLBENZOIC ACID;Dirnate;4-SULFAMYLBENZOIC ACID;P-SULFAMOYLBENZOIC ACID;4-CARBOXYBENZENESULPHONAMIDE;NSC2675;Carzenid;NSC 2675;NSC-2675;CARZENIDE
CBNumber:
CB9220906
Molecular Formula:
C7H7NO4S
Molecular Weight:
201.2
MDL Number:
MFCD00007938
MOL File:
138-41-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:20:27

Carzenide Properties

Melting point 285-295 °C (lit.)
Boiling point 449.0±47.0 °C(Predicted)
Density 1.5083 (rough estimate)
refractive index 1.6100 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility 0.5g/l
form Powder
pka 3.50(at 25℃)
color White
Water Solubility 453 mg/L (25 ºC)
Merck 14,1876
BRN 1875393
InChI 1S/C7H7NO4S/c8-13(11,12)6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)(H2,8,11,12)
InChIKey UCAGLBKTLXCODC-UHFFFAOYSA-N
SMILES O=S(C(C=C1)=CC=C1C(O)=O)(N)=O
CAS DataBase Reference 138-41-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 30Z5HQB5A4
NIST Chemistry Reference P-sulfamoylbenzoic acid(138-41-0)
EPA Substance Registry System 4-Aminosulfonylbenzoic acid (138-41-0)
UNSPSC Code 12352108
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-20/21/22
Safety Statements  22-24/25-36/37/39-26-36
WGK Germany  3
RTECS  DH6820000
TSCA  TSCA listed
HazardClass  IRRITANT
HS Code  29163990
Storage Class 11 - Combustible Solids
Toxicity LD50 i.p. in rats: 350 ± 22 mg/kg (Appenroth, Brunlich)
NFPA 704
1
2 0

Carzenide price More Price(65)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich C11804 4-Sulfamoylbenzoic acid 97% 138-41-0 5g $40.4 2026-04-30 Buy
Sigma-Aldrich C11804 4-Sulfamoylbenzoic acid 97% 138-41-0 100g $229 2026-04-30 Buy
TCI Chemical S0323 4-Sulfamoylbenzoic Acid >95.0%(T) 138-41-0 25g $25 2026-04-30 Buy
TCI Chemical S0323 4-Sulfamoylbenzoic Acid >95.0%(T) 138-41-0 500g $250 2026-04-30 Buy
Usbiological 289488 4-Sulfamylbenzoic acid Asreported 138-41-0 250g $372 2026-06-03 Buy
Product number Packaging Price Buy
C11804 5g $40.4 Buy
C11804 100g $229 Buy
S0323 25g $25 Buy
S0323 500g $250 Buy
289488 250g $372 Buy

Carzenide Chemical Properties,Uses,Production

Description

4-Sulfamoylbenzoic acid is a significant class of compounds extensively investigated for their potential applications across various disciplines. Characterized by a nitrogen-containing ring structure, 4-Sulfamoylbenzoic acid is a heterocyclic compound adorned with diverse substituents encircling the ring. Within the body, 4-Sulfamoylbenzoic acid is an agonist for several receptors, including those for serotonin and dopamine. By forming connections with these receptors, 4-Sulfamoylbenzoic acid proficiently modulates their functionality, consequently inducing changes in receptor behavior. This, in turn, precipitates an array of effects contingent upon the specific receptor and the studied drug.

Chemical Properties

White powder

Uses

diuretic, carbonic anhydrase inhibitor

Uses

4-Sulfamoylbenzoic Acid (Carzenide) is used as a reagent in the synthesis of carbonic anhydrase inhibitors anticonvulsant agents.

Definition

ChEBI: Carzenide is a sulfonamide.

Application

Carzenide is an antispasmodic that has been used in the treatment of dysmenorrhoea. Currently Carzenide is an organic synthesis intermediate, used for synthetic drug.

reaction suitability

reagent type: cross-linking reagent

Synthesis

p-Toluenesulfonamide

70-55-3

Carzenide

138-41-0

Example 11: In a 25 mL reaction vial, 1 mmol of p-carboxybenzenesulfonamide, 0.05 mmol of 3,5-dinitro-N-hydroxy-N-methylbenzamide, and 0.01 mmol of cobalt acetate were added, followed by the addition of 5 mL of acetic acid as solvent. The reaction system was placed in an oxygen atmosphere, maintaining an oxygen pressure of 1 atmosphere, and the temperature was raised to 100 °C. The reaction lasted for 10 hours. After completion of the reaction, the reaction mixture was cooled to room temperature. Recovery of acetic acid was achieved by removing acetic acid from the filtrate by distillation under reduced pressure. The residue was washed repeatedly with water to remove residual acetic acid and cobalt acetate co-catalyst, and then washed with a small amount of acetone to remove 3,5-dinitro-N-hydroxy-N-methylbenzamide and a small amount of p-hydroxymethylbenzenesulfonimide. The resulting filter cake was dried to give p-carboxybenzenesulfonamide. The yield of the reaction was 94.05%, the conversion of p-toluenesulfonamide was 99.33% and the selectivity of p-carboxybenzenesulfonamide was 94.68%. The product was analyzed by Agilent 1200 HPLC and the purity was 95.14%.

References

[1] Patent: CN105801455, 2016, A. Location in patent: Paragraph 0048
[2] Patent: US2004/58977, 2004, A1. Location in patent: Page/Page column 8; 14
[3] American Chemical Journal, 1885, vol. 7, p. 147
[4] Justus Liebigs Annalen der Chemie, 1875, vol. 178, p. 284
[5] Journal of the Chemical Society, 1951, p. 1877,1880

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View Lastest Price from Carzenide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Carzenide pictures 2026-09-02 Carzenide
138-41-0
$1.00-100.00 1KG 99% Henan Fengda Chemical Co., Ltd
Carzenide pictures 2026-05-28 Carzenide
138-41-0
$10.00 1KG 99% 10 ton Hebei Chuanghai Biotechnology Co,.LTD
Carzenide pictures 2026-04-22 Carzenide
138-41-0
$29.00 98.65% 10g TargetMol Chemicals Inc.
  • Carzenide pictures
  • Carzenide
    138-41-0
  • $1.00-100.00
  • 99%
  • Henan Fengda Chemical Co., Ltd
  • Carzenide pictures
  • Carzenide
    138-41-0
  • $10.00
  • 99%
  • Hebei Chuanghai Biotechnology Co,.LTD
  • Carzenide pictures
  • Carzenide
    138-41-0
  • $29.00
  • 98.65%
  • TargetMol Chemicals Inc.
P-CARBOXYBENZENESULFONAMIDE 4-(aminosulfonyl)-benzoicaci Benzoic acid, 4-(aminosulfonyl)- Benzoic acid, p-sulfamoyl- Carzenid Dirnate 4-sulphamoylbenzoic acid p-Caroxybenzenesulfonamide 4-carboxybebzenesulfonamide 4-Sulfomyl Benzoic Acid P-Carboxylbenzenesulfonamide p-Sulfamidobenzoic acid p-Caroxybenzenesulfonamide (Carzenide) 4-CARBOXYBENZESULFONAMIDE SULFAMOYLBENZOICAICD 4-Sulfamidobenzonium acid 4-Carboxybenzenesulfonamide, Benzoic acid 4-sulfamide 4-Carboxybenzenesulfonamide ,97% 4-Carboxybenzenesulfonamide (4-Sulfamoylbenzoic acid) 4-Carboxybenzenesulfonamide,95% 4-Sulfamoylbenzoic acid,4-Carboxybenzenesulfonamide, Benzoic acid 4-sulfamide 4-Carboxybenzenesulfonamide Carzenide SulfaMylbenzoic aci 4-SulfaMoylbenzoic acid 97% 4-Carboxybenzenesulfonamide for synthesis p-sulfamoyl-benzoicaci TIMTEC-BB SBB003533 4-(Aminosulphonyl)benzoic acid~4-Carboxybenzenesulphonamide~Carzenide RARECHEM AL BO 0772 P-SULFONAMIDOBENZOIC ACID P-SULFAMOYLBENZOIC ACID P-SULFAMYLBENZOIC ACID 4-(aminosulfonyl)- 4-SULFAMIDOBENZOIC ACID 4-SULFAMYLBENZOIC ACID 4-SULPHAMIDOBENZOIC ACID 4-SULFONAMIDOBENZOIC ACID 4-CARBOXYBENZENESULPHONAMIDE 4-CARBOXYBENZENESULFONAMIDE 4-(AMINOSULFONYL)BENZOIC ACID BENZOIC ACID 4-SULFAMIDE BENZOIC ACID P-SULFAMIDE BUTTPARK 148\07-58 CARZENIDE LABOTEST-BB LT00053349 Para Carboxy Benzene Sulphonamide 4-sulfamoylbenzoate 4-SulfamoylbenzoicAcid> Carzenide ISO 9001:2015 REACH BRN 1703866 NSC 2675 NSC2675 NSC-2675 Carzenide, 98+% Para Carboxy Benzene Sulfonamide p-Sulfonamidebenzoic acid Carzenide, 10 mM in DMSO Sulfonamide benzoic acid