Ordering
Available Variants5 g
CHA.78261-5g
Price
€68.00
Available – Dispatch in 14 days
25 g
CHA.78261-25g
Price
€271.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.78261-5g | €68.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.78261-25g | €271.20 |
BioXtra, suitable for cell culture
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) | C16H18N3NaO4S |
|---|---|
| CAS Number | 69-52-3 |
| Molecular Weight | 371.39 |
| UNSPSC Code | 51281716 |
| NACRES | NA.76 |
| PubChem Substance ID | 24891335 |
| EC Number | 200-708-1 |
| Beilstein/REAXYS Number | 4119211 |
| MDL number | MFCD00064313 |
Safety Information Handling visibility
| pictograms |
GHS08
 GHS08
|
|---|---|
| signalword | Danger |
| hcodes | H317,H334 |
| pcodes | P261 - P272 - P280 - P284 - P302 + P352 - P333 + P313 |
| 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 |
Technical Overview & Applications Use-case context
Ampicillin sodium salt, with a CAS number of 69-53-4, is a broad-spectrum antibiotic that belongs to the penicillin class. It is a sodium salt form of ampicillin, which enhances its solubility in water, making it more suitable for intravenous or intramuscular administration. Ampicillin sodium salt exhibits bactericidal activity against a wide range of Gram-positive and Gram-negative bacteria, including strains that produce beta-lactamase. Its mechanism of action involves inhibiting bacterial cell wall synthesis, ultimately leading to cell lysis and death. This antibiotic is commonly used to treat various infections, such as respiratory tract infections, urinary tract infections, and meningitis, particularly in cases where the causative organism is susceptible to ampicillin. The sodium salt form is often preferred due to its improved stability and pharmacokinetic properties.
