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CAS RN: 7177-48-2 | Product Number: A2092
Ampicillin Trihydrate
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Purity: >98.0%(T)(HPLC)
Synonyms:
- D-(-)-α-Aminobenzylpenicillin Trihydrate
Product Documents:
| Size | Unit Price | Philadelphia, PA | Portland, OR | Japan* | Quantity |
Shipping Information
|
|---|---|---|---|---|---|---|
| 5G |
$22.00
|
Contact Us | Contact Us | ≥40 |
|
|
| 25G |
$63.00
|
1 | Ships from Philadelphia the same day* | 33 |
|
* Items in stock locally typically ship the same day of ordering. Items from Japan stock are able to ship from a US warehouse within 2 weeks after ordering. For additional estimated shipment times, please refer to the Shipping Simulation tool. Note: Excludes regulated items and items that ship on ice.
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*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Supplemental Product Information:
This product has not been tested for potency and is guaranteed for chemical purity.
| Product Number | A2092 |
Purity / Analysis Method 
|
>98.0%(T)(HPLC) |
| Molecular Formula / Molecular Weight | C__1__6H__1__9N__3O__4S·3H__2O = 403.46 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Refrigerated (0-10°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 7177-48-2 |
| Related CAS RN
|
69-53-4 |
| Reaxys Registry Number | 5399534 |
| PubChem Substance ID | 87560211 |
| Merck Index (14) | 586 |
| MDL Number | MFCD00072036 |
Specifications
| Appearance | White to Orange to Green powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Nonaqueous Titration) | min. 98.0 %(calcd.on anh.substance) |
| Specific rotation [a]20/D | +280.0 to +305.0 deg(C=0.5, H2O)(calcd.on anh.substance) |
| Water | 12.0 to 15.0 % |
Properties (reference)
| Melting Point | 202 °C(dec.) |
| Specific Rotation | 293° (C=0.5,H2O) |
| Degree of solubility in water | 10 g/l 21 °C |
| Solubility (insoluble in) | Benzene, Chloroform, Ether |
GHS
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. H362 : May cause harm to breast-fed children. |
| Precautionary Statements | P263 : Avoid contact during pregnancy/ while nursing. P260 : Do not breathe dusts or mists. P270 : Do not eat, drink or smoke when using this product. P201 : Obtain special instructions before use. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P302 + P352 : IF ON SKIN: Wash with plenty of soap and water. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. P362 : Take off contaminated clothing and wash before reuse. |
Related Laws:
| RTECS# | XH8425000 |
Transport Information:
| HS Number | 2941.90.3000 |
Application
Ampicillin: The First of Broad Spectrum Penicillins
Ampicillin, a penicillin-like antibiotic, is enzymatic synthesized from 6-APA [A0800] catalyzed by penicillin acylase. Ampicillin is the first of a number of so-called broad spectrum penicillins. That amino group helps the drug penetrate the outer membrane of Gram-negative bacteria. Thus, ampicillin has activity against not only Gram-positive bacteria such as Staphylococci and Streptococci but also Gram-negative bacteria such as H. influenzae, coliforms and Proteus species. It acts as a competitive inhibitor of the enzyme transpeptidase, which is needed by bacteria to make their cell walls. Its spectrum of activity is enhanced by co-administration of sulbactam [S0868], a drug that inhibits beta lactamase an enzyme produced by bacteria to inactivate ampicillin. Ampicillin is used in molecular biology as a selective reagent most commonly to isolate bacteria coupled to a gene coding for ampicillin resistance, which is one of the most frequently used selection markers for obtaining transgenic cells.
References
- Ampicillin [D-6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid] (a review)
- Sulbactam/ampicillin. A review of its antibacterial activity, pharmacokinetic properties, and therapeutic use
- Ampicillin-sulbactam: an update on the use of parenteral and oral forms in bacterial infections
- Construction and characterization of new cloning vehicle. II. A multipurpose cloning system
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