跳转至内容
Merck
CN

S6377

磺胺异噁唑

≥99.0%

别名:

4-氨基- N -(3,4-甲基-3-异恶唑基)苯磺酰胺, N 1 -(3,4-二甲基-5-异恶唑基)磺胺, 磺胺异恶唑

登录 查看组织和合同定价。

选择规格

变更视图

关于此项目

经验公式(希尔记法):
C11H13N3O3S
化学文摘社编号:
分子量:
267.30
EC Number:
204-858-9
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
6737262
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


assay

≥99.0%

solubility

acetone: complete 50 mg/ml, 10% HCl: complete 33 mg/mL, clear, colorless to faintly yellow, alcohol: slightly soluble, chloroform: insoluble

originator

Roche

storage temp.

2-8°C

SMILES string

Cc1noc(NS(=O)(=O)c2ccc(N)cc2)c1C

InChI

1S/C11H13N3O3S/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6,14H,12H2,1-2H3

InChI key

NHUHCSRWZMLRLA-UHFFFAOYSA-N

Gene Information

rat ... Ednra(24326)

Application

Sulfisoxazole was one of the antibiotics tested on bacterial reporter panel that gave information on pollution load on the environment.11

Biochem/physiol Actions

Sulfisoxazole, a sulfonamide, is an antibacterial agent that acts by inhibiting the folic acid metabolism.1 It is also a non-selective endothelin antagonist. It is effective in the treatment of recurrent acute otitis media and also in rendering protection to retina against ischemic-like insults.2,3

Features and Benefits

This compound was developed by Roche. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.


Still not finding the right product?

Explore all of our products under 磺胺异噁唑


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库