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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
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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
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
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
Sigma-Aldrich
Product number
S340510
Product name
N4-ACETYL-N1-(4-NITROPHENYL)-SULFANILAMIDE, TECH.
Purity
Aldrich
Packaging
250mg
Price
$179
Updated
2024/03/01
Sigma-Aldrich
Product number
46882
Product name
Sulfanitran
Purity
VETRANAL?, analytical standard
Packaging
50mg
Price
$47.7
Updated
2022/05/15
Sigma-Aldrich
Product number
46882
Product name
Sulfanitran
Purity
VETRANAL?, analytical standard
Packaging
10mg
Price
$35.5
Updated
2022/05/15
TRC
Product number
S689040
Product name
Sulfanitran
Packaging
5g
Price
$1210
Updated
2021/12/16
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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

Career Henan Chemical Co
Product
SULFANITRAN 122-16-7
Price
US $1.00/KG
Min. Order
1KG
Purity
99.0%
Supply Ability
100kg
Release date
2020-01-18

122-16-7, SULFANITRANRelated Search:


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