TIANFU-CHEM 368-16...

TIANFU-CHEM  368-16-1  3-METHYL-L-HISTIDINE N-HYDRATE

TIANFU-CHEM 368-16-1 3-METHYL-L-HISTIDINE N-HYDRATE

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  • Purity: 99%min
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Keywords

368-16-1 3-METHYL-L-HISTIDINE N-HYDRATE C7H13N3O3

Quick Details

  • Appearance:conform
  • Application:368-16-1
  • PackAge:normal package
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:conform
  • Transportation:by 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

 

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1. Higest quality and good package

2.Fast delivery

3.Better payment term

4.Fast response to customer  within 6 hours

5.Good business credit in Europe ,US ,Japan ,Korea

 

Anyway ,if you need any chemicals from China ,Henan Tianfu can help you

Details:

3-METHYL-L-HISTIDINE N-HYDRATE Basic information
Product Name: 3-METHYL-L-HISTIDINE N-HYDRATE
Synonyms: 3-methylhistidine;3-METHYL-L-HISTIDINE N-HYDRATE;π-methyl-l-histidine;(2S)-2-amino-3-(3-methylimidazol-4-yl)propanoic acid;METHYL-L-HISTIDINE, 1-(RG);METHYL-L-HISTIDINE, 3-(RG);1-METHYL-L-HISTIDINE CRYSTALLINE;H-His(p-Me)-OH
CAS: 368-16-1
MF: C7H13N3O3
MW: 187.2
EINECS: 206-704-6
Product Categories: Amino Acids;Chiral Compound;amino acid
Mol File: 368-16-1.mol
3-METHYL-L-HISTIDINE N-HYDRATE Structure
 
3-METHYL-L-HISTIDINE N-HYDRATE Chemical Properties
density  1.37
storage temp.  Store at RT.
CAS DataBase Reference 368-16-1(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
MSDS Information
 
 
3-METHYL-L-HISTIDINE N-HYDRATE Usage And Synthesis
Usage 3-N-Methyl-L-histidine is a potential compound to be used as a treatment with pharmacological PPARα agonists to stimulate the ubiquitin proteasome pathway and myofibrillar protein breakdown in skeleta l muscle of rodents.

 

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