Valacyclovir hydrochloride

Suppliers

Names

[ CAS No. ]:
124832-27-5

[ Name ]:
Valacyclovir hydrochloride

[Synonym ]:
2-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)ethyl ester monohydrochloride
MFCD01861507
2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl L-valinate hydrochloride
L-Valine 2-(2-Amino-1,6-dihydro-6-oxo-9H-purin-9-ylmethoxy)ethyl Ester Hydrochloride Hydrate
Valaciclovir
2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl valinate hydrochloride (1:1)
2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl-(2S)-2-amino-3-methylbutanoathydrochlorid
2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate hydrochloride
Valacyclovir hydrochloride
Zelitrex
Valaciclovir hydrochloride
(2S)-2-amino-3-méthylbutanoate de 2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)méthoxy]éthyle chlorhydrate
Valaciclovir HCl
256u
L-Valine 2-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)ethyl ester monohydrochloride
Valine, 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]ethyl ester, hydrochloride (1:1)
Valacyclovir hydrochloride hydrate
Valacyclovir (hydrochloride)

Chemical & Physical Properties

[ Density]:
1.55g/cm3

[ Boiling Point ]:
588.4ºC at 760 mmHg

[ Melting Point ]:
170-172ºC

[ Molecular Formula ]:
C13H21ClN6O4

[ Molecular Weight ]:
360.797

[ Flash Point ]:
309.7ºC

[ Exact Mass ]:
360.131287

[ PSA ]:
151.14000

[ LogP ]:
1.28590

[ Vapour Pressure ]:
7.95E-14mmHg at 25°C

[ Index of Refraction ]:
1.673

[ Storage condition ]:
Refrigerator

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ Precautionary Statements ]:
P301 + P312 + P330

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Precursor

  • Cbz-Valacyclovir
  • Valacyclovir
  • Acyclovir
  • 9-(2'-ACETOXYETHOXYMETHYL)GUANINE

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Oral antiviral therapy for prevention of genital herpes outbreaks in immunocompetent and nonpregnant patients.

Cochrane Database Syst. Rev. 8 , CD009036, (2014)

Genital herpes is caused by herpes simplex virus 1 (HSV-1) or 2 (HSV-2). Some infected people experience outbreaks of genital herpes, typically, characterized by vesicular and erosive localized painfu...

Acute retinal necrosis associated with Epstein-Barr virus: immunohistopathologic confirmation.

JAMA Ophthalmol. 132(7) , 881-2, (2014)

Acute retinal necrosis (ARN) is an infectious retinitis primarily caused by the herpesviruses. Although the Epstein-Barr virus (EBV) has been implicated as a cause of ARN, to our knowledge, there has ...

A pilot study examining the safety and tolerability of valacyclovir in veterans with hepatitis C virus/herpes simplex virus type 2 coinfection.

Am. J. Med. Sci. 348(6) , 455-9, (2014)

We performed a pilot study examining the safety and tolerability of valacyclovir in veterans with herpes simplex virus type 2 and hepatitis C virus (HCV) coinfection.We performed a randomized double-b...


More Articles


Related Compounds

  • valacyclovir hydrochloride
  • D-Valacyclovir Hydrochloride
  • Valacyclovir hydrochloride hydrate
  • N-Ethyl valacyclovir hydrochloride
  • N-Methyl valacyclovir hydrochloride
  • Valacyclovir hydrochloride dihydrate
  • 1-(5-Amino-1,2,3,4-tetrahydroisoquinolin-2-yl)-3-methylbutan-1-one
  • 1-(5-Amino-1,2,3,4-tetrahydroisoquinolin-2-yl)-2,3-dimethylbutan-1-one
  • 3-Chloro-4-methoxy-N-(3-(methylsulfonyl)propyl)aniline
  • 4-(3,3,3-Trifluoropropylamino)piperidine-4-carboxamide
  • Ethyl 1-(2-fluoropyridin-3-yl)-5-hydroxy-1H-pyrazole-3-carboxylate
  • 4-[[(4-Fluorophenyl)methyl]amino]-4-piperidinecarboxamide
  • [4-(3-Methylsulfonylpropoxy)phenyl]methanamine
  • 2-Acetyl-4-chloro-2H-indazole
  • Ethyl 5-(3-methylbutan-2-yl)-1,2,4-oxadiazole-3-carboxylate
  • 5-(3-Methylbutan-2-yl)-1,2,4-oxadiazole-3-carboxylic acid
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