BATRACHOTOXIN

BATRACHOTOXIN Suppliers list
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:BTX
CAS:23509-16-2
Purity:NLT 98% Remarks:MC543250
Company Name: GIHI CHEMICALS CO.,LIMITED
Tel: +8618058761490
Email: info@gihichemicals.com
Products Intro: Product Name:1H-Pyrrole-3-carboxylicacid, 2,4-dimethyl-,(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-
CAS:23509-16-2
Purity:99 Package:5KG;1KG,25kg
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 821-50328103-801 18930552037
Email: 3bsc@sina.com
Products Intro: Product Name:Batrachotoxin;(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-Dodecahydro-9,12-dihydroxy-2-11a-diMethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl2,4-diMethyl-1H-pyrrole-3-carboxylate
CAS:23509-16-2
Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:Batrachotoxin
CAS:23509-16-2
Purity:>95% Package:10mg
Company Name: Tocris Bioscience  
Tel: +44 (0) 117 916 3333
Email: customerservice@tocris.co.uk
Products Intro: Product Name:Batrachotoxin;(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-Dodecahydro-9,12-dihydroxy-2-11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl2,4-dimethyl-1H-pyrrole-3-carboxylate
CAS:23509-16-2
BATRACHOTOXIN Basic information
Product Name:BATRACHOTOXIN
Synonyms:Batrachotoxinin A, 20-(2,4-dimethyl-1H-pyrrole-3-carboxylate);C13750;(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-Dodecahydro-9,12-dihydroxy-2-11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl2,4-dimethyl-1H-pyrrole-3-carboxylate;BATRACHOTOXIN;1H-Pyrrole-3-carboxylic acid, 2,4-dimethyl-, (1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-f][1,4]oxazepin-14-yl]ethyl ester;ISNYUQWBWALXEY-OMIQOYQYSA-N;BTX;1H-Pyrrole-3-carboxylicacid, 2,4-dimethyl-,(1S)-1-[(5aR,7aR,9R,11aS,11bS,12R,13aR)-1,2,3,4,7a,8,9,10,11,11a,12,13-dodecahydro-9,12-dihydroxy-2,11a-dimethyl-7H-9,11b-epoxy-13a,5a-propenophenanthro[2,1-
CAS:23509-16-2
MF:C31H42N2O6
MW:538.67
EINECS:
Product Categories:Sodium channel
Mol File:23509-16-2.mol
BATRACHOTOXIN Structure
BATRACHOTOXIN Chemical Properties
alpha 24584 -5 To -10°; 24300 -260° (c = 0.23 in methanol)
Boiling point 614.87°C (rough estimate)
density 1.1575 (rough estimate)
refractive index 1.5800 (estimate)
storage temp. Store at -20°C
pka7.45(at 25℃)
form Thin film.
color Noncrystal
CAS DataBase Reference23509-16-2
EPA Substance Registry SystemBetrachotoxinin A, 20-.alpha.-(2,4-dimethyl-1H-pyrrole-3-carboxylate) (23509-16-2)
Safety Information
RIDADR 3172
HazardClass 6.1(b)
PackingGroup III
Hazardous Substances Data23509-16-2(Hazardous Substances Data)
ToxicityLD50 s.c. in mice: 2 mg/kg (Tokuyama)
MSDS Information
BATRACHOTOXIN Usage And Synthesis
Chemical PropertiesNoncrystal.
HazardExtremely toxic; deadly poison; neurotoxic; cardiotoxic activity; bara-chotoxin that blocks neuromuscular transmission; respiratory paralysis; death.
Biological ActivityPotent neurotoxin that activates voltage-gated sodium channels. Shifts voltage-dependent activation to more negative potentials, inactivation is disabled and pore conductance and selectivity are altered (displays increased permeability for NH 4 + , K + and Cs + ions).
Safety ProfileA deadly poison byintraperitoneal, intravenous, and subcutaneous routes.When heated to decomposition it emits toxic fumes ofNOx.
Enzyme inhibitorThis lipid-soluble neurotoxin (FW = 526.67 g/mol; CAS 23509-16-2; LD50 = ~2 μg/kg mouse body weight.), isolated from the skin of the Columbian poison-dart frog Phyllobates aurotaenis, enhances Na+ conductance, promoting opening of voltage-gated Na+ channels, inducing depolarization of the resting membrane potential. It does so by binding to the sodium channel, keeping the membrane permeable to sodium ions in an all-or-none manner. This results in hyperexcitability of excitable tissues, followed by convulsions, paralysis, and death in animals. The most common use of batrachotoxin is in darts for bloguns used in hunting by the Noanamá Chocó and Emberá Chocó Indians of western Colombia. Batrachotoxin has also been identified in the feathers of the passerine birds of New Guinea Pitohui dichrous, Pitohui kirhocephalus, and Ifrita kowaldi. The less toxic batrachotoxin A is the deesterified steroid.
BATRACHOTOXIN Preparation Products And Raw materials
Tag:BATRACHOTOXIN(23509-16-2) Related Product Information
Tetracaine hydrochloride Aconitine VERATRIDINE TETRODOTOXIN QX-314 L-KAWAIN PD 85639 DIHYDROCARVEOL (+)-ISOPULEGOL (-)-DIHYDROCARVEOL BETA-TERPINEOL 2,5-DIMETHYL-1,5-HEXADIEN-3-OL BATRACHOTOXIN homobatrachotoxin CIS-2-AMINOMETHYL-1-METHYL-CYCLOHEXANOL 1-ALLYL-1-METHOXY-CYCLOHEXANE (E)-4-ETHOXY-NONA-1,5-DIENE 2-METHOXY-2-METHYL-BUT-3-EN-1-OL