氯霉素

发表于由

氯霉素

γ辐照

有货

氯霉素

CAS编号 56-75-7 | 品牌：Jinpan
Chloramphenicol

MSDS

质检证书(CoA)

相似产品

  • 分子式 C11H12Cl2N2O5
  • 分子量323.13
  • Beilstein号 2225532
  • EC号 200-287-4
  • PubChem编号 5959

货号 (SKU) 包装规格 是否现货 价格 数量
C432942-20mg 20mg 期货 氯霉素  

基本信息

产品名称 氯霉素
英文名称 Chloramphenicol
别名 Chloromycetin, D(−)-threo-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-β-(4-nitrophenyl)ethyl]acetamide, D-(−)-threo-2-Dichloroacetamido-1-(4-nitrophenyl)-1,3-propanediol, D-threo-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-4-nitrophenethyl]acetamide
英文别名 D-(−)-threo-2-Dichloroacetamido-1-(4-nitrophenyl)-1,3-propanediol, D-(−)-threo-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-β-(4-nitrophenyl)ethyl]acetamide, Chloromycetin, D-threo-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymeth
规格或纯度 γ辐照
运输条件 冰袋运输
生化机理 Mode of Action: Inhibits translation on the 50S ribosomal subunit at the peptidyltransferase step (elongation inhibition). Bacteriostatic. Mode of Resistance: Acetylation by chloramphenicol acetyltransferase ( cat gene).

一般描述

制备说明

直接用小瓶配制推荐范围内任意浓度的储存液。储存液应在 Store at 2-8°C 下保存。在 37°C 下可稳定 5 天。

Gene Information

human … CYP1A2(1544)

General Description

Chemical structure: phenicole

Application

Chloramphenicol is a synthetic antibiotic, isolated from strains of Streptomyces venezuelae. It is often used for bacterial selection in molecular biology applications at 10-20 μg/mL and as a selection agent for transformed cells containing chloramphenicol reistance genes.

Other Notes

Keep container tightly closed in a dry and well-ventilated place. Light sensitive.

相关属性

CAS编号 56-75-7
比旋光度 20 ° (C=5, EtOH)
熔点 149-153°C
溶解性 无水乙醇：5-20mg/mL（作为储备溶液）；甲醇：可溶（作为储备溶液）
储存温度 2-8°C储存
RTECS AB6825000
分子量 323.13
分子式 C11H12Cl2N2O5
EC号 200-287-4
品牌 Jinpan
备注 注意: Stock solutions should be stored at Store at 2-8°C and are stable at 37°C for 5 days. Aqueous solutions are neutral and stable over a wide pH range, with 50% hydrolysis occurring after 290 days. Use of a borax buffered solution reduces this number to 14%
Smiles OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+](=O)[O-];OC[C@H](NC(=O)C(Cl)Cl)[C@H](O)c1ccc(cc1)[N+](=O)[O-];OCC(/N=C(O)/C(Cl)Cl)C(O)c1ccc(cc1)[N+](=O)[O-];OCC(NC(=O)C(Cl)Cl)C(O)c1ccc(cc1)[N+](=O)[O-]
PubChem CID 5959