Ordering
Available Variants5 g
CHA.57204-5g
Price
€37.84
Available – Dispatch in 14 days
25 g
CHA.57204-25g
Price
€145.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.57204-5g | €37.84 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.57204-25g | €145.60 |
900-1050 μg/mg anhydrous basis (HPLC)
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.85 |
| PubChem Substance ID | 57653869 |
| 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 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| 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 |
| wgk | WGK 2 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
Technical Overview & Applications Use-case context
Ampicillin trihydrate, with a CAS number of 69-53-4, is a semi-synthetic beta-lactam antibiotic derived from penicillin. It exhibits a broad spectrum of antibacterial activity, effectively inhibiting the growth of both Gram-positive and Gram-negative bacteria. The trihydrate form of ampicillin is commonly used in pharmaceutical applications due to its increased stability and solubility. As a cell wall synthesis inhibitor, ampicillin trihydrate works by binding to penicillin-binding proteins, ultimately leading to the disruption of bacterial cell wall formation and resulting in bacterial cell lysis. This mechanism of action renders ampicillin trihydrate an effective treatment option for various bacterial infections, including those of the respiratory and urinary tracts, as well as skin and soft tissue infections, when used under the guidance of a healthcare professional. Its efficacy and safety profile make it a widely used antibiotic in clinical settings.
