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CAS RN: 23325-78-2 | Product Number: C2248

Cephalexin Monohydrate


Purity: >98.0%(HPLC)
Synonyms:
  • Cefalexin Monohydrate
Product Documents:
5G
$110.00
4   2   25  
25G
$329.00
1   1   9  

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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 Pictogram
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.
P280 : Wear protective gloves.
P272 : Contaminated work clothing must not be allowed out of the workplace.
P302 + P352 : IF ON SKIN: Wash with plenty of soap and water.
P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention.
P363 : Wash contaminated clothing before reuse.
Related Laws:
RTECS# XI0350000
Transport Information:
HS Number 2941.10.5000
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


PubMed Literature


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