METHENAMINE MANDELA...

METHENAMINE MANDELATE

METHENAMINE MANDELATE

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1 Kilogram

FOB Price: USD 30.0000

  • Min.Order :1 Kilogram
  • Purity: 90.0%Min
  • Payment Terms : L/C,T/T,

Keywords

587-23-5 METHENAMINE MANDELATE METHENAMINE MANDELATE

Quick Details

  • Appearance:Powder
  • Application:For pharmacy chemiacals
  • PackAge:As per customer's
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:Room Temperature
  • Transportation:By sea air

Superiority:

Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:
 
1.Noble Metal Catalysts (Pt.Pd...)
2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)
3.OLED intermediates (Fluorene,Carbazole,Boric acid...)
4.Customs Synthesis
 
Our advantage:
 
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Details:

Product Name: METHENAMINE MANDELATE
Synonyms: METHENAMINE MANDELATE;METHENAMINE MANDELATE SALT;HEXAMINE MANDELATE SALT;HEXAMETHYLENETETRAMINE MANDELATE;HEXAMETHYLENETETRAMINE MANDELATE SALT;1,3,5,7-TETRAAZATRICYCLO-[3.3.1.1(3)(7)]DECANE MANDELATE SALT;HEXAMINEMANDELATE;Methenamine Mandelate (200 mg)
CAS: 587-23-5
MF: C14H20N4O3
MW: 292.33
EINECS: 209-597-4
Product Categories: Heterocyclic Compounds
Mol File: 587-23-5.mol
METHENAMINE MANDELATE Structure
METHENAMINE MANDELATE Chemical Properties
Melting point  128-130°
Fp  250℃
CAS DataBase Reference 587-23-5(CAS DataBase Reference)
Safety Information
WGK Germany  3
HS Code  2933690000
MSDS Information
Provider Language
SigmaAldrich English
METHENAMINE MANDELATE Usage And Synthesis
Uses Antibacterial (urinary).
Brand name Mandelamine (Parke-Davis).
Clinical Use Hexamethylenetetramine mandelate (Methenamine) is awhite crystalline powder with a sour taste and practically noodor. It is very soluble in water and has the advantage ofproviding its own acidity, although in its use, the custom isto carry out a preliminary acidification of the urine for 24 to36 hours before administration.

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