N4-Acetylsulfadimethoxine
| Code | Size | Price |
|---|
| CDX-A0298-M025 | 25 mg | £205.00 |
Quantity:
| CDX-A0298-M100 | 100 mg | £596.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
N(4)-AcSDM; 4-Acetylamino-N-(4,6-dimethoxy-pyrimidin-2-yl)benzenesulfonamide; N4-Acetyl-N1-(4,6-dimethoxy-2-pyrimidinyl)sulfanilamide
Appearance:
Off-white powder.
CAS:
555-25-9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H315, H317, H319, H335
InChi:
InChI=1S/C14H16N4O5S/c1-9(19)15-10-4-6-11(7-5-10)24(20,21)18-12-8-13(22-2)17-14(16-12)23-3/h4-8H,1-3H3,(H,15,19)(H,16,17,18)
InChiKey:
WIYOSEJTAADVPJ-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 555-25-9. Formula: C14H16N4O5S. MW: 352.37. Synthetic Metabolite of the long-acting sulfonamide antibiotic sulfadimethoxine, used in freshwater aquaculture. Sulfonamide that is benzenesulfonamide substituted by an acetylamino group at position 4 and a 4,6-dimethoxy-pyrimidin-2-yl group at the nitrogen atom. Compound can be used as analytical reference material.
MDL:
MFCD00580046
Molecular Formula:
C14H16N4O5S
Molecular Weight:
352.37
Package Type:
Vial
Precautions:
P261, P280, P305, P351, P338
Product Description:
Metabolite of the long-acting sulfonamide antibiotic sulfadimethoxine, used in freshwater aquaculture. Sulfonamide that is benzenesulfonamide substituted by an acetylamino group at position 4 and a 4,6-dimethoxy-pyrimidin-2-yl group at the nitrogen atom. Compound can be used as analytical reference material.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
COC1=NC(OC)=NC(NS(=O)(=O)C2=CC=C(NC(C)=O)C=C2)=C1
Solubility Chemicals:
Soluble in chloroform.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) Y. Imamura, et al.; Chem. Pharm. Bull. 31, 274 (1983) | (2) Y. Imamura, et al.; Chem. Pharm. Bull. 35, 1299 (1987) | (3) Y. Imamura, et al.; Eur. J. Drug Metab. Pharmacokinet. 12, 169 (1987) | (4) M. Otagiri, et al.; Chem. Pharm. Bull. 37, 498 (1989) | (5) J.J. Guerard, et al.; Environ. Sci. Technol. 43, 8587 (2009)
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