一二三四区视频,亚洲少妇熟女色,日本久热无码视频网,欧美国产日韩大尺度,亚洲a视频,久久少妇一区二区,日韩999无码视频,刺激久久久久久久,啊啊啊啊不要啊在线

ChemicalBook >> CAS DataBase List >>Valacyclovir hydrochloride

Valacyclovir hydrochloride

CAS No.
124832-27-5
Chemical Name:
Valacyclovir hydrochloride
Synonyms
VALACYCLOVIR;VALACICLOVIR HCL;VALACICLOVIR HYDROCHLORIDE;Valtrex;Valacyclovir hydrochloride hydrate;256U;VALACV;BW 256;Zelitrex;BW 256U87
CBNumber:
CB8430566
Molecular Formula:
C13H20N6O4.ClH
Molecular Weight:
360.8
MDL Number:
MFCD01861507
MOL File:
124832-27-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-03 11:24:09
Product description Number Pack Size Price
Valaciclovir for system suitability European Pharmacopoeia (EP) Reference Standard Y0001225 10 mg $127
Valaciclovir hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard Y0000834 210 mg $167
Valacyclovir HCl Pharmaceutical Secondary Standard; Certified Reference Material PHR1601 1g $201
Valacyclovir hydrochloride British Pharmacopoeia (BP) Reference Standard BP1194 100mg $259
Valacyclovir hydrochloride United States Pharmacopeia (USP) Reference Standard 1707839 200mg $463
More product size

Valacyclovir hydrochloride Properties

Melting point 170-172°C
storage temp. Keep in dark place,Sealed in dry,Store in freezer, under -20°C
solubility H2O: >20mg/mL
form solid
color white
Water Solubility H2O: >20mg/mL
λmax 253nm(H2O)(lit.)
Merck 14,9899
Stability Hygroscopic
InChI InChI=1/C13H20N6O4.ClH/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20;/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20);1H/t8-;/s3
InChIKey ZCDDBUOENGJMLV-JNODIIHCNA-N
SMILES C(N1C=NC2C(N=C(NC=21)N)=O)OCCOC(=O)[C@@H](N)C(C)C.Cl |&1:18,r|
CAS DataBase Reference 124832-27-5(CAS DataBase Reference)
FDA UNII G447S0T1VC
NCI Drug Dictionary valacyclovir hydrochloride
UNSPSC Code 41116107
NACRES NA.32

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-22
Safety Statements  26-36-24/25
RIDADR  3077
WGK Germany  3
HS Code  29335990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
NFPA 704
0
2 0

Valacyclovir hydrochloride price More Price(90)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0001225 Valaciclovir for system suitability European Pharmacopoeia (EP) Reference Standard 124832-27-5 10 mg $127 2026-04-30 Buy
Sigma-Aldrich Y0000834 Valaciclovir hydrochloride (anhydrous) European Pharmacopoeia (EP) Reference Standard 124832-27-5 210 mg $167 2026-04-30 Buy
Sigma-Aldrich PHR1601 Valacyclovir HCl Pharmaceutical Secondary Standard; Certified Reference Material 124832-27-5 1g $201 2026-04-30 Buy
Sigma-Aldrich BP1194 Valacyclovir hydrochloride British Pharmacopoeia (BP) Reference Standard 124832-27-5 100mg $259 2026-04-30 Buy
Sigma-Aldrich 1707839 Valacyclovir hydrochloride United States Pharmacopeia (USP) Reference Standard 124832-27-5 200mg $463 2026-04-30 Buy
Product number Packaging Price Buy
Y0001225 10 mg $127 Buy
Y0000834 210 mg $167 Buy
PHR1601 1g $201 Buy
BP1194 100mg $259 Buy
1707839 200mg $463 Buy

Valacyclovir hydrochloride Chemical Properties,Uses,Production

Description

Valacyclovir hydrochloride, an orally active L-valyl ester of the potent antiviral agent aciclovir, was launched in 1995 in the United Kingdom for the treatment of herpes simplex virus (HSV) infections of the skin and mucous membranes, including initial and recurrent genital herpes. As a prodrug, valaciclovir has an improved pharmacokinetic profile to aciclovir. It is rapidly absorbed after oral administration and extensively converted to aciclovir via first-pass metabolism to achieve plasma levels of aciclovir comparable to those seen with aciclovir via i.v. route. Valacyclovir is then activated selectively in virus-infected cells by viral thymidine kinase to form aciclovir triphosphate in a stepwise fashion. This active species inhibits viral DNA polymerase via irreversible binding to the active site of the enzyme. Once aciclovir is incorporated into the elongating viral DNA, it terminates replication of the viral DNA strand, an antiviral mechanism unique to aciclovir. Valacyclovir is reportedly in clinical trials for the suppression of cytomegalovirus infection and disease in renal transplant patients.

Chemical Properties

White Crystalline Powder

Originator

Glaxo Wellcome (United Kingdom)

History

Valacyclovir hydrochloride is an antiviral drug developed by GlaxoSmithKline and marketed under the brand name Valtrex. It was first approved by the FDA in June 2001 for the treatment of infections caused by the herpes simplex virus (HSV), including genital herpes, cold sores, and shingles in adults, as well as cold sores in children.

Uses

Acyclovir (A192400) impurity. The L-Valine ester prodrug of Acyclovir.

Uses

Valaciclovir hydrochloride is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.

Definition

ChEBI: Valacyclovir hydrochloride is an organic molecular entity.

brand name

Valtrex (GlaxoSmithKline).

General Description

Valacyclovir (Valtrex) is the hydrochloride salt of the Lvalylester of acyclovir. The compound is a water-solublecrystalline solid, and it is a prodrug intended to increase thebioavailability of acyclovir by increasing lipophilicity.Valacyclovir is hydrolyzed rapidly and almost completely toacyclovir following oral administration.
Valacyclovir has been approved for the treatment of herpeszoster (shingles) in immunocompromised patients. Theside effect profile observed in valacyclovir is comparablewith bioequivalent doses of acyclovir.

Pharmacokinetics

The binding of valacyclovir to human plasma proteins ranges between 13.5 to 17.9%. The plasma elimination half-life of acyclovir is 2.5 to 3.3 hours. The bioavailability of valacyclovir hydrochloride is 54%, compared to approximately 20% for oral acyclovir, and it is as effective as acyclovir in decreasing the duration of pain associated with posttherapeutic neuralgia and episodes of genital lesion healing.

Side effects

The adverse effects are similar to acyclovir, which include nausea, headache, vomiting, constipation, and anorexia.

Synthesis

Cbz-Valaciclovir

124832-31-1

Valacyclovir hydrochloride

124832-27-5

General procedure: To a 1L hydrogenation kettle was added (S)-2-((2-amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl 2-(((benzyloxy)carbonyl)amino)-3-methylbutanoate (50g), concentrated hydrochloric acid (9.6mL), 5% palladium-carbon catalyst (5g) and water (350mL), and the reaction was carried out for 6 to 12 hours under the conditions of hydrogen pressure of 3kg/cm2 and temperature of 25-30°C. -30°C for 6 to 12 hours. Upon completion of the reaction, the reaction mixture was vacuum filtered and the filter cake was washed with water. The filtrate was concentrated under reduced pressure and subsequently cooled to room temperature. Isopropanol was added to the concentrate, which was further cooled to 5-10 °C and maintained at that temperature for 1 hour. The precipitated solid was (S)-2-((2-amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl 2-amino-3-methylbutyrate hydrochloride, which was filtered and washed with cold isopropanol to give the product. The yield was 92% and the purity was 99.8%. Analytical conditions: Chromatographic column: USP L1, 4.6×150 mm, 3.5 μm (Zorbax SB-C18, item 863953-914) Detector: UV 250nm Mobile phase A: In a 1000mL volumetric flask, add 2.8mL triethylamine with 800mL ultrapure water, adjust pH to 5.00±0.05 with glacial acetic acid, and settle to scale. Mobile phase B: acetonitrile Injection volume: 50μL Column temperature: 30°C Flow rate: 1.0mL/min Gradient elution

References

[1] Asian Journal of Chemistry, 2010, vol. 22, # 5, p. 4092 - 4098
[2] Patent: WO2013/76688, 2013, A1. Location in patent: Page/Page column 10-11
[3] Patent: US2014/296520, 2014, A1. Location in patent: Paragraph 0043
[4] Journal of Pharmaceutical Sciences, 2001, vol. 90, # 10, p. 1505 - 1515
[5] Patent: WO2006/35452, 2006, A1. Location in patent: Page/Page column 5-6

124832-31-1
124832-27-5
Synthesis of Valacyclovir hydrochloride from Cbz-Valaciclovir

Valacyclovir hydrochloride Preparation Products And Raw materials

Global( 582)Suppliers
Supplier Tel Email Country ProdList Advantage
shandong perfect biotechnology co.ltd
+86-53169958659 +86-13153181156 sales@sdperfect.com China 294 58
Anhui Ruihan Technology Co., Ltd
+8617756083858 daisy@anhuiruihan.com China 973 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 20122 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618092446649 sarah@tnjone.com China 1143 58
Hebei Zhuanglai Chemical Trading Co.,Ltd
+8613343047651 admin@zlchemi.com China 3692 58
Hefei Lbao Physical & Chemical Science Co.,Ltd
+15184799099 lbaochemicals@gmail.com China 670 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29640 60
Beijing Cooperate Pharmaceutical Co.,Ltd
010-60279497 sales01@cooperate-pharm.com CHINA 1803 55
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21586 55
Shanghai Yingrui Biopharma Co., Ltd.
+86-21-33585366 - 03@ sales03@shyrchem.com CHINA 738 60

View Lastest Price from Valacyclovir hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Valacyclovir hydrochloride pictures 2026-06-11 Valacyclovir hydrochloride
124832-27-5
0.99 RongNa Biotechnology Co.,Ltd
Valacyclovir hydrochloride pictures 2026-06-02 Valacyclovir hydrochloride
124832-27-5
$32.00-98.00 98.65% 10g TargetMol Chemicals Inc.
Valacyclovir hydrochloride pictures 2026-06-02 Valacyclovir hydrochloride
124832-27-5
$32.00-98.00 98.65% 10g TargetMol Chemicals Inc.

Valacyclovir hydrochloride Spectrum

2-[(2-azanyl-6-oxo-3H-purin-9-yl)methoxy]ethyl (2S)-2-azanyl-3-methyl-butanoate hydrochloride L-Valacyclovir Hydrochloride Valacyclovir Hydrochloride (200 mg) L-Valine, 2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]ethyl ester, monohydrochloride (9CI) VALACYCLOVIR HYDROCHLORIDE [9-((2-HYDROXY-ETHOXY)MET HYL)GUANINE L-VALINE ESTER HYDROCHLORIDE] (S)-2-((2-AMINO-6-OXO-1H-PURIN-9(6H)-YL)METHOXY)ETHYL 2-AMINO-3-METHYLBUTANOATE HYDROCHLORIDE 9-((2-Hydroxy-ethoxy)methyl)guanine L-valine ester hydrochloride (2S)-2-amino-3-methyl-butyric acid 2-[(2-amino-6-keto-3H-purin-9-yl)methoxy]ethyl ester hydrochloride 2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]ethyl (2S)-2-amino-3-methylbutanoate hydrochloride L-VALINE 2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9YL)METHOXY]ETHYL ESTER, HYDROCHLORIDE SALT VALACV VALACYCLOVIR HYDROCHLORIDE L-Valine 2-[(2-AMino-1,6-dihydro-6-oxo-9H-purin-9yl)Methoxy]ethyl Ester Hydrochlroride Salt Zelitrex L-Valine 2-(2-Amino-1,6-dihydro-6-oxo-9H-purin-9-ylmethoxy)ethyl Ester Hydrochloride L-Valine-2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]ethyl ester, hydrochloride (1:1) Valaciclovir hydrochloride (anhydrous) Valaciclovir for system suitability 2-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)ethyl ester monohydrochloride L-Valacyclovir HCl (S)-2-[(2-Amino-6-oxo-6,9-dihydro-3H-purin-9-yl)methoxy]ethyl-2-amino-3-methylbutanoate Valaciclovir Hydrochloride Tablets\n VALACICLOVIR HCL 99% VALACICLOVIR HYDROCHLORIDE,98.0+% VALACYCLOVER HYDROCHLORIC 98+% L-VALINE -2-[(2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL) METHOXY]ETHYLESTER MONOHYDROCHLORIDE Valacycloverhydrochloride L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Ester, Hydrochlroride Salt, ValACV VALACYCLOVER HYDROCHLORIC 256U 256U87 hydrochloride BW 256 BW 256U87 Valacyclovir hydrochloride, 98%, HSV antagonist 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl-L-valinate hydrochloride Valaciclovir for system suitability CRS Valaciclovir Hydrochloride RS Valaciclovir hydrochloride (anhydrous) CRS Valaciclovir, hydrochloride salt L-Valine 2-[(2-Amino-1,6-dihydro-6-oxo-9H-purin-9yl)methoxy]ethyl Valacyclovir hydrochloride USP/EP/BP Valganciclovir hydrochloride salt Valaciclovir for system suitability (Y0001225)Q: What is Valaciclovir for system suitability (Y0001225) Q: What is the CAS Number of Valaciclovir for system suitability (Y0001225) Valaciclovir hydrochloride (anhydrous) (Y0000834) Valacyclovir HydrochlorideQ: What is Valacyclovir Hydrochloride Q: What is the CAS Number of Valacyclovir Hydrochloride Q: What is the storage condition of Valacyclovir Hydrochloride Q: What are the applications of Valacyclovir Hydrochloride valacyclovir API Valacyclovir Hydrochloride (1707839) Vanaclovir hydrochloride Valtrex Valacyclovir hydrochloride hydrate VALACICLOVIR HCL VALACICLOVIR HYDROCHLORIDE VALACYCLOVIR 2H5]-Valganciclovir hydrochloride salt 2-[(2-Amino-6-oxo-1H-purin-9(6H)-yl)methoxy]ethyl (S)-2-Amino-3-methylbutanoate Hydrochloride Valciclovir hydrochloride Vannamelovir hydrochloride Valacicloviri hydrochloridum
临漳县| 四会市| 二连浩特市| 丰城市| 广汉市| 尼玛县| 延川县| 侯马市| 府谷县| 彭泽县| 洛南县| 德兴市| 花莲市| 莎车县| 抚州市| 平果县| 柘荣县| 吴旗县| 西充县| 东乌珠穆沁旗| 宽城| 江源县| 塘沽区| 张家界市| 长垣县| 岫岩| 罗城| 故城县| 永吉县| 会昌县| 廉江市| 丹巴县| 报价| 封丘县| 金平| 株洲县| 秦安县| 海南省| 仁寿县| 宁陕县| 昌江|