Ordering
Available Variants25 g
CHA.95679-25g
Price
€152.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.95679-25g | €152.00 |
meets USP testing specifications
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C16H19N3O4S · 3H2O |
|---|---|
| CAS Number | 7177-48-2 |
| Molecular Weight | 403.45 |
| UNSPSC Code | 51281703 |
| NACRES | NA.76 |
| PubChem Substance ID | 24890564 |
| EC Number | 200-709-7 |
| Beilstein/REAXYS Number | 5399534 |
| MDL number | MFCD00072036 |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
  GHS08,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H315,H317,H319,H334,H335 |
| Hazard Classifications | Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
Technical Overview & Applications Use-case context
Ampicillin, with the chemical formula C16H19N3O4S and CAS number 69-53-4, is a beta-lactam antibiotic that functions by inhibiting bacterial cell wall synthesis. It is a broad-spectrum antibiotic, effective against a wide range of Gram-positive and Gram-negative bacteria, including certain strains of Escherichia, Salmonella, and Shigella. Ampicillin is commonly used to treat various infections, such as pneumonia, urinary tract infections, and meningitis, particularly in cases where the causative organism is susceptible to the antibiotic. The mechanism of action involves binding to penicillin-binding proteins, resulting in the disruption of the bacterial cell wall and ultimately leading to cell lysis and death. Resistance to ampicillin can occur through various mechanisms, including the production of beta-lactamase enzymes that degrade the antibiotic.
