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CAS RN: 134678-17-4 | Product Number: L0217

Lamivudine


Purity: >98.0%(T)(HPLC)
Synonyms:
  • 3TC
  • (-)-1-[(2R,5S)-2-(Hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine
Documents:
100MG
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Note:

This product is a sample for RUO (research use only). Do not use this product for any purpose other than testing and research.

Product Number L0217
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__8H__1__1N__3O__3S = 229.25 
Physical State (20 deg.C) Solid
Storage Temperature Frozen (<0°C)
Condition to Avoid Heat Sensitive
Packaging and Container 1G-Glass Bottle with Plastic Insert (View image)
CAS RN 134678-17-4
Reaxys Registry Number 5480511
PubChem Substance ID 87560180
Merck Index (14) 5352
MDL Number

MFCD00869739

Specifications
Appearance White to Almost white powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Nonaqueous Titration) min. 98.0 %
Melting point 175.0 to 179.0 °C
Specific rotation [a]20/D -137.0 to -147.0 deg(C=1, methanol)
Properties (reference)
Melting Point 177 °C
Specific Rotation -142° (C=1,MeOH)
Solubility in water Soluble
Degree of solubility in water 70,000 mg/l   20 °C
Solubility (soluble in) Methanol
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H373 : May cause damage to organs through prolonged or repeated exposure.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P260 : Do not breathe dust/ fume/ gas/ mist/ vapors/ spray.
P314 : Get medical advice/ attention if you feel unwell.
Related Laws:
RTECS# UW7361333
Transport Information:
Application
Lamivudine: An L-Nucleoside Reverse Transcriptase Inhibitor

Lamivudine is a nucleoside reverse transcriptase inhibitor that active against HIV1, HIV2, and hepatitis B. Lamivudine is a synthetic L-nucleoside analogue of the naturally occurring D-nucleoside 2’-deoxycytidine. Intracellularly, lamivudine is converted by cellular enzymes to the active metabolite, lamivudine-5'-triphosphate. The triphosphate inhibits the activity of viral reverse transcriptase both by competing with the natural substrate, 2’-deoxycytidine-5'-triphosphate, and by its incorporation into viral DNA causing termination of viral DNA chain. (The product is for research purpose only.)

References


PubMed Literature


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