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(3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate is a potent neurotoxic chemical compound derived from plants in the grayanotoxin family, such as rhododendrons and azaleas. It is composed of a butanoate molecule attached to a grayanotoxin molecule, which features multiple hydroxyl groups attached to a complex carbon ring structure. (3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate is known for its neurotoxic effects, which can cause symptoms like dizziness, nausea, vomiting, and potentially fatal cardiac arrhythmias upon ingestion. Due to its toxic nature, it is crucial to handle (3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate with extreme caution to prevent ingestion or exposure.

84849-09-2

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84849-09-2 Usage

Uses

Used in Research and Development:
(3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate is used as a research compound for studying its neurotoxic properties and potential applications in understanding the effects of grayanotoxins on the nervous system. (3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate can provide insights into the development of antidotes or treatments for poisoning caused by plants in the grayanotoxin family.
Used in Pharmaceutical Development:
Although the compound itself is highly toxic, it may be used as a starting point for the development of pharmaceuticals targeting specific neurological conditions. Researchers can study the compound's interaction with the nervous system to develop safer and more effective drugs with similar mechanisms of action but reduced toxicity.
Used in Toxicology Studies:
(3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate can be employed in toxicology studies to better understand the mechanisms of grayanotoxin poisoning and to develop strategies for prevention and treatment. This can include the study of the compound's effects on various organ systems, as well as the development of diagnostic tools and treatment protocols for poisoning incidents.
Used in Environmental and Wildlife Protection:
Understanding the toxic effects of (3beta,6beta)-3,5,6,9,16-pentahydroxygrayanotoxan-14-yl butanoate can contribute to the development of guidelines and safety measures for the protection of wildlife and the environment. This can include the creation of educational materials to inform the public about the risks associated with grayanotoxin-containing plants and the implementation of strategies to minimize exposure to these toxins.

Check Digit Verification of cas no

The CAS Registry Mumber 84849-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,4 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84849-09:
(7*8)+(6*4)+(5*8)+(4*4)+(3*9)+(2*0)+(1*9)=172
172 % 10 = 2
So 84849-09-2 is a valid CAS Registry Number.

84849-09-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4a,8,11,11a-pentahydroxy-1,1,4,8-tetramethyltetradecahydro-7,9a-methanocyclopenta[b]heptalen-12-yl butyrate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84849-09-2 SDS

84849-09-2Upstream product

84849-09-2Downstream Products

84849-09-2Relevant academic research and scientific papers

Quantitative Structure-Inotropy Relationship Applied to Substituted Grayanotoxins

Shirai, Naohiro,Sakakibara, Jinsaku,Kaiya, Toyo,Kobayashi, Sawako,Hotta, Yoshihiro,Takeya, Kazumi

, p. 851 - 855 (2007/10/02)

Nine 14β-O-acylated grayanotoxins were synthesized by ozonolysis of 14,16-alkylidenegrayanotoxin III.The correlation between positive inotropic potency (PIE) in guinea pigs and physicochemical parameters (Vw, Mw, and Rm50) in 14,14-substituted

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