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About This Item
InChI key
KLOHDWPABZXLGI-YWUHCJSESA-M
InChI
1S/C16H19N3O4S.Na/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);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
SMILES string
[Na+].CC1(C)SC2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C([O-])=O
biological source
synthetic (chemical)
form
powder
color
white to off-white
mp
215 °C (dec.) (lit.)
solubility
water: 50 g/L
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
application(s)
agriculture
mode of action
cell wall synthesis | interferes
storage temp.
2-8°C
Quality Level
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Related Categories
General description
Application
- to select for ampicillin resistance in mutated and transformed cells
Biochem/physiol Actions
Mode of Resistance: Administration with β-lactamase cleaves the β-lactam ring of Ampicillin and inactivates it.
Antimicrobial Spectrum: Includes both gram-positive (similar to benzylpenicillin) and gram-negative bacteria (similar to tetracyclines and chloramphenicol.
Features and Benefits
- High-quality antibiotic suitable for multiple research applications
- Ideal for Cell Biology and Biochemical research.
Preparation Note
Other Notes
Disclaimer
signalword
Danger
hcodes
Hazard Classifications
Resp. Sens. 1A - Skin Sens. 1A
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
A9518-VAR-9: + A9518-BULK-9: + A9518-25G-9: + A9518-5G:4548173188287 + A9518-BULK: + A9518-100G:4548173188263 + A9518-6X100G:4548173188294 + A9518-VAR: + A9518-25G:4548173188270
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細胞培養ラボの安全性を適切に維持する方法の概要:ラボのリスク評価、機材表面の消毒、バイオハザードや廃棄手順についてECACC handbook無料ダウンロード。
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