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CAS RN: 23325-78-2 | Product Number: C2248
Cephalexin Monohydrate
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Purity: >98.0%(HPLC)
Synonyms:
- Cefalexin Monohydrate
Product Documents:
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* The storage conditions are subject to change without notice.
* The storage conditions are subject to change without notice.
Supplemental Product Information:
This product has not been tested for potency and is guaranteed for chemical purity.
Product Number | C2248 |
Purity / Analysis Method | >98.0%(HPLC) |
Molecular Formula / Molecular Weight | C__1__6H__1__7N__3O__4S·H__2O = 365.41 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 23325-78-2 |
Related CAS RN | 15686-71-2 |
Reaxys Registry Number | 4072576 |
PubChem Substance ID | 87560315 |
Merck Index (14) | 1974 |
MDL Number | MFCD00167148 |
Specifications
Appearance | White to Orange to Green powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Nonaqueous Titration) | min. 97.0 % |
Specific rotation [a]20/D | +149 to +158 deg(C=0.5, H2O)(calcd.on anh.substance) |
Water | 4.0 to 8.0 % |
Properties (reference)
Specific Rotation | 154° (C=0.5,H2O) |
GHS
Pictogram |
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Signal Word | Warning |
Hazard Statements | H317 : May cause an allergic skin reaction. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P261 : Avoid breathing dust. P272 : Contaminated work clothing should not be allowed out of the workplace. P280 : Wear protective gloves. P302 + P352 : IF ON SKIN: Wash with plenty of water. P362 + P364 : Take off contaminated clothing and wash it before reuse. P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention. |
Related Laws:
RTECS# | XI0350000 |
Transport Information:
H.S.code* | 2941.90-000 |
Application
Cephalexin: The Most Popular First-Generation Semisynthetic Cephalosporin Antibiotic
Cephalexin is the most popular first-generation semisynthetic cephalosporin antibiotic, which is chemically synthesized form 7-aminodesacetoxycephalosporanic acid (7-ADCA) [A2075]. It has a broad spectrum of activity against Gram-positive and Gram-negative bacteria. The side chain substituents on the cephalosporin nucleus are the same as the substituents on the penicillin nucleus of ampicillin [A2092]. Cephalexin attains much higher serum concentrations than ampicillin in equivalent oral doses and is much less bound to serum proteins than cephalothin [C2769].
References
- Cephalexin. A review of its antibacterial, pharmacological and therapeutic properties
- Review of the spectrum and potency of orally administered cephalosporins and amoxicillin/clavulanate
PubMed Literature
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