Supply 3,5-Dimethyl...

Supply 3,5-Dimethylpiperidine 35794-11-7 C7H15N by China manufacture

Supply 3,5-Dimethylpiperidine 35794-11-7 C7H15N by China manufacture

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 98% purity
  • Payment Terms : L/C,D/A,D/P,T/T,Other

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Offer 35794-11-7 35794-11-7 Best quality 35794-11-7

Quick Details

  • Appearance:white powder
  • Application:35794-11-7
  • PackAge:By 5g/10g/25g bags or as customer's request .
  • ProductionCapacity:10|Metric Ton|Month
  • Storage:Under room tempearture condition .
  • Transportation:by courier /by sea / by air

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3,5-Dimethylpiperidine Basic information
Product Name: 3,5-Dimethylpiperidine
Synonyms: 3,5-dimethyl-piperidin;3,5-dimethylpiperidine,mixtureofcisandtrans;3,5-DIMETHYLPIPERIDINE;35LPT;3,5-LUPETIDINE;AKOS BBS-00003678;HEXAHYDRO-3,5-LUTIDINE;3,5-Lupeptidine
CAS: 35794-11-7
MF: C7H15N
MW: 113.2
EINECS: 252-730-6
Product Categories: Piperidine;Building Blocks;C5 to C7;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines
Mol File: 35794-11-7.mol
3,5-Dimethylpiperidine Structure
 
3,5-Dimethylpiperidine Chemical Properties
bp  144 °C(lit.)
density  0.853 g/mL at 25 °C(lit.)
refractive index  n20/D 1.4454(lit.)
Fp  91 °F
storage temp.  Flammables area
BRN  102638
CAS DataBase Reference 35794-11-7(CAS DataBase Reference)
NIST Chemistry Reference Piperidine, 3,5-dimethyl-(35794-11-7)
EPA Substance Registry System Piperidine, 3,5-dimethyl-(35794-11-7)
 
Safety Information
Hazard Codes  Xi,F
Risk Statements  10-36/37/38
Safety Statements  16-26-36/37/39-37/39-36
RIDADR  UN 1993 3/PG 3
WGK Germany  3
HazardClass  3
PackingGroup  III
MSDS Information
Provider Language
3,5-Dimethylpiperidine English
ACROS English
SigmaAldrich English
ALFA English
 
3,5-Dimethylpiperidine Usage And Synthesis
Chemical Properties clear colorless to light yellow liquid
Usage Reactant for synthesis of: Substituted bisphenol A derivatives as β-amyloid peptide aggregation inhibitors1 MMP-13 selective isonipecotamide α-sulfone hydroxamates2 Gem-diamines for active organocatalysts for biodiesel production3 Benzimidazole inhibitors of the antigen receptor-mediated NF-κB4 Reactant for Mannich reactions to form Ru(II) complexes5

 

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