跳转至内容

尊敬的客户:

目前国际形势复杂多变,关税政策尚不明朗,这可能对我们的产品价格产生一定影响。在此情况下,我们希望就订单事宜与您进行友好沟通。

基于当前的不确定性,如果您选择在此期间下单,我们将保留根据实际情况调整价格的权利。同时,我们也理解市场变化可能给您带来的困扰,因此如果在订单实际发货前因关税政策变动导致价格出现较大波动,默克将与您进行协商讨论并视情况对订单进行调整或取消。

Merck
CN
所有图片(1)

主要文件

安全信息

A6140

Sigma-Aldrich

氨苄西林 三水合物

900-1050 μg/mg anhydrous basis (HPLC)

别名:

氨苄青霉素

登录查看公司和协议定价

选择尺寸

100 G
¥512.23
500 G
¥1,031.59

¥512.23


预计发货时间2025年4月27日详情


获取大包装报价

选择尺寸

变更视图
100 G
¥512.23
500 G
¥1,031.59

About This Item

经验公式(希尔记法):
C16H19N3O4S · 3H2O
CAS号:
分子量:
403.45
Beilstein:
5399534
EC 号:
MDL编号:
UNSPSC代码:
51281703
PubChem化学物质编号:
NACRES:
NA.85

¥512.23


预计发货时间2025年4月27日详情


获取大包装报价

质量水平

表单

powder or crystals

浓度

900-1050 μg/mg (anhydrous, HPLC)

mp

198-200 °C (dec.) (lit.)

抗生素抗菌谱

Gram-negative bacteria
Gram-positive bacteria

作用机制

cell wall synthesis | interferes

储存温度

2-8°C

SMILES字符串

O.O.O.CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(O)=O

InChI

1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1

InChI key

RXDALBZNGVATNY-CWLIKTDRSA-N

正在寻找类似产品? 访问 产品对比指南

比较类似商品

查看完整比较结果

显示差异

1 of 4

此商品
PHR139331591A1593
氨苄西林 meets USP testing specifications

A1593

氨苄西林

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

antibiotic activity spectrum

-

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

antibiotic activity spectrum

Gram-negative bacteria, Gram-positive bacteria

Quality Level

200

Quality Level

300

Quality Level

100

Quality Level

200

form

powder or crystals

form

-

form

-

form

solid

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

concentration

900-1050 μg/mg (anhydrous, HPLC)

concentration

-

concentration

-

concentration

-

mp

198-200 °C (dec.) (lit.)

mp

198-200 °C (dec.) (lit.)

mp

198-200 °C (dec.) (lit.)

mp

198-200 °C (dec.) (lit.)

一般描述

化学结构:β-内酰胺

应用

氨苄西林三水合物通常用于选择突变和转化细胞中的氨苄西林抗性。

生化/生理作用

一种具有连接到青霉素结构上的氨基侧链的 β-内酰胺抗生素。通过灭活细菌细胞膜内表面的转肽酶而抑制细菌细胞壁合成(肽聚糖交联)的青霉素衍生物。仅对生长中的大肠埃希菌具有杀菌作用。耐药方式:氨苄西林的 β-内酰胺环被 β-内酰胺酶裂解。抗菌谱:革兰阴性菌和革兰阳性菌。

其他说明

保存于密闭容器内,置于干燥通风处。

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

监管及禁止进口产品
  • 技术规格说明书

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

    没有发现合适的版本?

    如果您需要特殊版本,可通过批号或批次号查找具体证书。

    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

    H J Nelis et al.
    Antimicrobial agents and chemotherapy, 36(8), 1606-1610 (1992-08-01)
    The determination of ampicillin in plasma and serum by reversed-phase high-performance liquid chromatography with UV detection suffers from poor selectivity and sensitivity. Currently, the most common approach to overcoming these problems consists of improving the compound's detectability via pre- or
    Ramendra K Singh et al.
    European journal of medicinal chemistry, 45(3), 1078-1086 (2009-12-26)
    Curcumin bioconjugates, viz. di-O-tryptophanylphenylalanine curcumin (2), di-O-decanoyl curcumin (3), di-O-pamitoyl curcumin (4), di-O-bis-(gamma,gamma)folyl curcumin (6), C(4)-ethyl-O-gamma-folyl curcumin (8) and 4-O-ethyl-O-gamma-folyl curcumin (10) have been synthesized and tested for their antibacterial and antiviral activities. The conjugates 2, 3, 4, 6 and
    Sherif A F Rostom et al.
    Bioorganic & medicinal chemistry, 17(2), 882-895 (2008-12-17)
    The synthesis of two groups of structure hybrids comprising basically the antipyrine moiety attached to either polysubstituted thiazole or 2,5-disubstituted-1,3,4-thiadiazole counterparts through various linkages is described. Twelve out of the newly synthesized compounds were evaluated for their anti-inflammatory activity using
    Ebtehal S Al-Abdullah et al.
    European journal of medicinal chemistry, 46(9), 4642-4647 (2011-08-19)
    New series of 6-phenyl-2,4-disubstituted pyrimidine-5-carbonitriles namely, 2-substitued thio-6-phenyl-3,4-dihydro-4-oxopyrimidine-5-carbonitriles (5a-d, 6, 7a-d, 8), 2-(4-chlorobenzylthio)-4-chloro-6-phenylpyrimidine-5-carbonitrile (9), 2-(4-chlorobenzylthio)-4-arylthio-6-phenylpyrimidine-5-carbonitriles (10a-d) and 2-(4-chlorobenzylthio)-4-arylamino-6-phenylpyrimidine-5-carbonitriles (11a-d) was synthesized and tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus
    Sherif A F Rostom et al.
    Bioorganic & medicinal chemistry, 17(6), 2410-2422 (2009-03-03)
    The azole pharmacophore is still considered a viable lead structure for the synthesis of more efficacious and broad spectrum antimicrobial agents. Potential antibacterial and antifungal activities are encountered with some tetrazoles. Therefore, this study presents the synthesis and antimicrobial evaluation

    我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

    联系客户支持