SULFANITRAN
- Product Name
- SULFANITRAN
- CAS No.
- 122-16-7
- Chemical Name
- SULFANITRAN
- Synonyms
- N-[4-[(4-nitrophenyl)sulfamoyl]phenyl]acetamide;APNPS;NSC-77120;NSC 217299;SULFANITRAN;sulfanitran85+%;Sulfanitran Standard;sulfanitranapprox.85%;C17000050 Sulfanitran;sulfanitran approx. 85%
- CBNumber
- CB4174763
- Molecular Formula
- C14H13N3O5S
- Formula Weight
- 335.34
- MOL File
- 122-16-7.mol
SULFANITRAN Property
- Melting point:
- 239-240° (Kaufmann); mp 264° (Shepherd)
- Density
- 1.500±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 7.42±0.10(Predicted)
- color
- yellow to greenish-yellow
- BRN
- 2952955
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- S340510
- Product name
- N4-ACETYL-N1-(4-NITROPHENYL)-SULFANILAMIDE, TECH.
- Purity
- Aldrich<sup>CPR</sup>
- Packaging
- 1 unit
- Price
- $185
- Updated
- 2025/07/31
- Product number
- S340510
- Product name
- N4-ACETYL-N1-(4-NITROPHENYL)-SULFANILAMIDE, TECH.
- Purity
- Aldrich
- Packaging
- 250mg
- Price
- $179
- Updated
- 2024/03/01
- Product number
- 46882
- Product name
- Sulfanitran
- Purity
- VETRANAL?, analytical standard
- Packaging
- 50mg
- Price
- $47.7
- Updated
- 2022/05/15
- Product number
- 46882
- Product name
- Sulfanitran
- Purity
- VETRANAL?, analytical standard
- Packaging
- 10mg
- Price
- $35.5
- Updated
- 2022/05/15
- Product number
- S689040
- Product name
- Sulfanitran
- Packaging
- 5g
- Price
- $1210
- Updated
- 2021/12/16
SULFANITRAN Chemical Properties,Usage,Production
Chemical Properties
Yellowish Green Solid
Uses
Sulfanitran is a sulfanomide derivative used as an anticoccidial drug. Sulfanitran is added to the drinking water of chickens as an aid in the treatment of coccidiosis caused by E. tenella, E. necatrix, and E. acervulina.
Uses
anti-hypertensive
Definition
ChEBI: N-[4-[(4-nitrophenyl)sulfamoyl]phenyl]acetamide is a sulfonamide.
Synthesis
100-01-6
121-60-8
122-16-7
GENERAL METHOD: To a solution of 4-nitroaniline (1 eq.) in pyridine (1.6 mL/mmol) was slowly added p-acetamidobenzenesulfonyl chloride (1.1 eq.) and the reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction was quenched with water and extracted three times with ethyl acetate (EtOAc). The organic layers were combined and washed sequentially with 0.5 N HCl three times, water three times and saturated saline once. The organic phase was dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure to give N-(4-(N-(4-nitrophenyl)aminosulfonyl)phenyl)acetamide as a solid product.
References
[1] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 18, p. 4426 - 4430
[2] Patent: US2282769, 1939,
[3] Journal of the American Chemical Society, 1939, vol. 61, p. 613,616
[4] DRP/DRBP Org.Chem.,
[5] Canadian Journal of Research, Section B: Chemical Sciences, 1942, vol. 20, p. 5,7, 9
SULFANITRAN Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from SULFANITRAN manufacturers
- Product
- SULFANITRAN 122-16-7
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99.0%
- Supply Ability
- 100kg
- Release date
- 2020-01-18