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HYPOXANTHINE 3-N-OXIDE, also known as an oxopurine, is a compound characterized by its 3,9-dihydro-6H-purine structure. It is substituted by an oxo group at position 6 and has a hydroxy group replacing the hydrogen attached to the nitrogen at position 3. This molecule is a significant component of Schreckstoff, an alarm pheromone found in fish.

19765-65-2

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19765-65-2 Usage

Uses

Used in Chemical Research:
HYPOXANTHINE 3-N-OXIDE is used as a research compound for studying the chemical properties and reactions of oxopurines. Its unique structure allows scientists to explore various aspects of its reactivity and potential applications in chemical synthesis.
Used in Pharmaceutical Industry:
HYPOXANTHINE 3-N-OXIDE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Environmental Studies:
In the field of environmental science, HYPOXANTHINE 3-N-OXIDE can be used as a biomarker to study the presence and impact of Schreckstoff, the alarm pheromone found in fish. This can help researchers understand the ecological role of this pheromone and its potential effects on aquatic ecosystems.
Used in Analytical Chemistry:
HYPOXANTHINE 3-N-OXIDE can be employed as a reference compound in analytical chemistry for the development and validation of new analytical methods. Its distinct chemical properties make it suitable for testing the accuracy and precision of various analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 19765-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19765-65:
(7*1)+(6*9)+(5*7)+(4*6)+(3*5)+(2*6)+(1*5)=152
152 % 10 = 2
So 19765-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N4O2/c10-5-3-4(7-1-6-3)9(11)2-8-5/h1-2,11H,(H,6,7)

19765-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Hypoxanthine 3-N-oxide

1.2 Other means of identification

Product number -
Other names 3-oxo-vobasan-17-oic acid methyl ester

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:19765-65-2 SDS

19765-65-2Downstream Products

19765-65-2Related news

Research reportThe synthetic substance HYPOXANTHINE 3-N-OXIDE (cas 19765-65-2) elicits alarm reactions in zebrafish (Danio rerio)09/02/2019

Zebrafish, one of the preferred study species of geneticists, is gaining increasing popularity in behavioral neuroscience. This small and prolific species may be an excellent tool with which the biological mechanisms of vertebrate brain function and behavior are investigated. Zebrafish has been ...detailed

19765-65-2Relevant academic research and scientific papers

Ostariophysan alarm pheromones: Laboratory and field tests of the functional significance of nitrogen oxides

Brown, Grant E.,Adrian Jr., James C.,Smyth, Erin,Leet, Heather,Brennan, Scott

, p. 139 - 154 (2007/10/03)

In laboratory and field-trapping studies, we exposed fathead minnows (Pimephales promelas) and finescale dace (Chrosomus neogaeus) to hypoxanthine-3-N-oxide and a suite of structurally and functionally similar compounds in order to determine if: (1) hypoxanthine-3-N-oxide functions as a chemical alarm signal in ostariophysan fishes and (2) the purine skeleton, a structural component, or the nitrogen oxide, a functional component, or both act as the molecular trigger in this chemical alarm signaling system. Minnows and dace exhibited significant antipredator responses when exposed to conspecific skin extract or hypoxanthine-3-N-oxide (increased shoaling and decreased area use) and the functionally similar pyridine-N-oxide (increased shoaling) but not to structurally similar molecules lacking a nitrogen oxide functional group or to a swordtail skin extract control. Field-trapping studies revealed similar results. Traps labeled with fathead minnows skin extract, hypoxanthine-3-N-oxide, or pyridine-N-oxide caught significantly fewer fish than did those labeled with distilled water. These data strongly suggest that the nitrogen oxide functional group acts as the chief molecular trigger in the Ostariophysan alarm pheromone system and that, contrary to previous research, hypoxanthine-3-N-oxide may be one of several possible molecules that function as a chemical alarm signal. Here we report the first example of a single functional group capable of eliciting a suite of behavioral responses.

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