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HENAN SUNLAKE ENTERPRISE CORPORATIONSTRYCHNINE HYDROCHLORIDE//file1.lookchem.com/cas/reactions/2021/05/25/4927442.png
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STRYCHNINE HYDROCHLORIDE CAS NO.1421-86-9

Min.Order Quantity:
1 Kilogram
Purity:
97%
Port:
China Main Port
Payment Terms:
L/C,D/A,D/P,T/T,MoneyGram,Other

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Product Details

Keywords

  • STRYCHNINE HYDROCHLORIDE
  • 1421-86-9
  • C21H23ClN2O2

Quick Details

  • ProName: STRYCHNINE HYDROCHLORIDE
  • CasNo: 1421-86-9
  • Molecular Formula: C21H23ClN2O2
  • Appearance: powder
  • Application: 1421-86-9
  • DeliveryTime: Within 3-7days
  • PackAge: As requested
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Day
  • Purity: 97%
  • Storage: store at R.T.
  • Transportation: By air or by sea
  • LimitNum: 1 Kilogram

Superiority

strychnine hydrochloride basic information
product name: strychnine hydrochloride
synonyms: strychnine hcl;strychnine hydrochloride;strychnidin-10-one,monohydrochloride;strychnine,monohydrochloride;strychnine hydrochloride hydrate;strychnidin-10-one, monohydrochloride (9ci);strychnidin-10-onehydrochloride
cas: 1421-86-9
mf: c21h23cln2o2
mw: 370.87
einecs: 215-826-9
product categories: chiral;alkaloids;biochemistry;for resolution of acids;indole alkaloids;optical resolution;synthetic organic chemistry;gaba and glycine receptor modulatorsneurotransmission;glycinergics;ion channels;ligand-gated ion channels;neurotransmitters
mol file: 1421-86-9.mol
strychnine hydrochloride structure
strychnine hydrochloride chemical properties
mp 295 °c
storage temp. store at rt
merck 8855
cas database reference 1421-86-9(cas database reference)
safety information
hazard codes t+,n
risk statements 26/27/28-51/53-50/53-26/28
safety statements 22-36/37/39-45-61-60-28-13
ridadr un 1692 6.1/pg 1
wgk germany 3
rtecs wl2430000
hazardclass 6.1(a)
packinggroup i
strychnine hydrochloride usage and synthesis
usage strychnine hydrochloride acts as an antagonist for cholinesterases and beta amyloid aggregation.
biological activity competitive glycine receptor antagonist; convulsant. also nicotinic receptor antagonist; displays competitive antagonism at α 7 receptors and non-competitive antagonism at α 4 β 2 receptors.

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