DETA-NONOate - ≥95% , CAS No.146724-94-9

CAS: 146724-94-9 Cat. No.: D670428 Molecular Weight: 163.18 EC Number: 633-925-9

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DETA-NONOate - ≥95% CAS No(146724-94-9) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY ≥95%

Synonyms

(Z)-1-[N-(2-Aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate | Diethylenetriamine NONOate;NOC-18 | DETA NONOate | 2,2′-(Hydroxynitrosohydrazono)bis-ethanimine

Storage

Protected from light,Argon charged,Desiccated,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product References Solution Calculators Reviews

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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Protected from light,Argon charged,Desiccated,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Store In the Dark. Store under desiccating conditions. This product is air and light sensitive and impurities can occur as a result of air oxidation or due to metabolism by microbes.

Application：

Diethylenetriamine/nitric oxide adduct has been used as nitric oxide (NO) donor:

to evaluate the direct effects of NO on cell proliferation in ovine trophectoderm (oTr1) cells;

to test its effects on recreating the growth inhibitory effect of NO without the presence of macrophages;

to correlate the outflow function and outflow tract vessel diameter changes with other controls in porcine models.

Specifications

Synonyms

(Z)-1-[N-(2-Aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1, 2-diolate | Diethylenetriamine NONOate;NOC-18 | DETA NONOate | 2, 2′-(Hydroxynitrosohydrazono)bis-ethanimine

Specifications & Purity

≥95%

Biochemical and Physiological Mechanisms

Nitric oxide donor. Able to spontaneously release NO (t 1/2 = 20 h). Also releases HNO. Decomposition is dependent on pH. Vasodilatory effects in vitro and in vivo . Cell-permeable.

Storage

Protected from light, Argon charged, Desiccated, Store at -80°C

Shipped In

Dry ice packs + Cold packs

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

Canonical Smiles	C(CN(CCN)[N+](=NO)[O-])N
IUPAC Name	(Z)-[bis(2-aminoethyl)amino]-hydroxyimino-oxidoazanium
InChIKey	YNRCBOXEDICOIX-CLFYSBASSA-N
INCHI	1S/C4H13N5O2/c5-1-3-8(4-2-6)9(11)7-10/h10H,1-6H2/b9-7-
Isomeric SMILES	C(CN(CCN)/[N+](=N/O)/[O-])N
WGK Germany	3
Molecular Weight	163.18
Reaxy-Rn	8140575
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8140575&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic 1,3-dipolar compounds
  - Class Allyl-type 1,3-dipolar organic compounds

Kingdom	Organic compounds
Superclass	Organic 1,3-dipolar compounds
Class	Allyl-type 1,3-dipolar organic compounds
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Allyl-type 1,3-dipolar organic compounds
Alternative Parents	Organopnictogen compounds Organic zwitterions Organic oxides Monoalkylamines Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as allyl-type 1,3-dipolar organic compounds. These are organic 1,3-dipolar compounds with the general structure X=Y+-Z- <-> X--Y+=Z<-> X+-Y-Z-<-> X-=Y-Z+ (X, Z = C, N, or O; Y = N or O).
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D Structure

Associated Targets(Human)

A498 (42825 Activities)

Lot Number	Certificate Type	Date	Item
E2431163	Certificate of Analysis	Feb 05, 2026	D670428
I2404343	Certificate of Analysis	Sep 20, 2024	D670428
E2431162	Certificate of Analysis	Jun 03, 2024	D670428

Solubility	Soluble in water
Sensitivity	Moisture、air and light sensitive
Molecular Weight	163.180 g/mol
XLogP3	-1.400
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	5
Exact Mass	163.107 Da
Monoisotopic Mass	163.107 Da
Topological Polar Surface Area	117.000 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	122.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1