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氨苄西林

产品号 10047 公司名称 Sigma Aldrich
CAS号 69-53-4 公司网站 http://www.sigmaaldrich.com
分子式 C16H19N3O4S 电 话 1-800-521-8956
分子量 349.40476 传 真
纯 度 ≥98.0% (NT) 电子邮件
保 存 Chembase数据库ID: 298

产品价格信息

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产品别名

标题
Ampicillin
IUPAC标准名
(2S,5R,6R)-6-[(2R)-2-amino-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
IUPAC传统名
ampicillin
别名
D-(-)-α-Aminobenzylpenicillin
氨苄青霉素

产品登记号

MDL号 MFCD00005175
Beilstein号 1090925
EC号 200-709-7
CAS号 69-53-4

产品性质

Empirical Formula (Hill Notation) C16H19N3O4S
杂质 ≤1% water
纯度 ≥98.0% (NT)
熔点 208 °C (dec.)(lit.)
比旋光度 [α]20/D +295±5°, c = 0.2% in H2O
溶解度 1 M NH4OH: soluble50 mg/mL, clear, colorless
GHS危险品标识 GHS07
GHS危险品标识 GHS08
GHS警示词 Danger
GHS危险声明 H315-H317-H319-H334-H335
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P261-P280-P305 + P351 + P338-P342 + P311
危险公开号 36/37/38-42/43
RTECS编号 XH8350000
安全公开号 22-26-36/37
保存温度 2-8°C
德国WGK号 2

产品详细信息

详细说明 (English)
Biochem/physiol Actions
A β-lactam antibiotic with an amino group attached to the penicillin structure. Inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli. Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.
Inhibits cell wall synthesis in Escherichia coli1; In the purification of penicillin acylase2; Enhances luminol chemiluminescence.3
详细说明 (简体中文)
Biochem/physiol Actions
A β-lactam antibiotic with an amino group attached to the penicillin structure. Inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli. Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.
Inhibits cell wall synthesis in Escherichia coli1; In the purification of penicillin acylase2; Enhances luminol chemiluminescence.3

参考文献