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3,3,5,5-Tetramethyl-1-pyrroline N-Oxide - >98.0%(GC), high purity , CAS No.10135-38-3

    Grade & Purity:
  • ≥98%(GC)
In stock
Item Number
T162332
Grouped product items
SKU Size
Availability
Price Qty
T162332-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$46.90
T162332-100mg
100mg
1
$76.90
T162332-250mg
250mg
1
$133.90

Basic Description

Synonyms NSC78027 | NSC-78027 | 2,2,4,4-Tetramethyl-3,4-dihydro-2H-pyrrole 1-oxide | 3,3,5,5-Tetramethyl-1-pyrroline N-oxide, 95% | AKOS015842131 | AS-69311 | DTXSID10143871 | SCHEMBL1420817 | 2,2,4,4-tetramethyl-1-oxido-3H-pyrrol-1-ium | 3,3,5,5-Tetramethyl-1-pyr
Specifications & Purity ≥98%(GC)
Storage Temp Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyrrolines
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Pyrrolines
Alternative Parents Nitrones  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Pyrroline - Nitrone - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as pyrrolines. These are compounds containing a pyrroline ring, which is a five-member unsaturated aliphatic ring with one nitrogen atom and four carbon atoms.
External Descriptors Not available

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 2,2,4,4-tetramethyl-1-oxido-3H-pyrrol-1-ium
INCHI InChI=1S/C8H15NO/c1-7(2)5-8(3,4)9(10)6-7/h6H,5H2,1-4H3
InChIKey GUQARRULARNYQZ-UHFFFAOYSA-N
Smiles CC1(CC([N+](=C1)[O-])(C)C)C
Isomeric SMILES CC1(CC([N+](=C1)[O-])(C)C)C
WGK Germany 3
PubChem CID 151490
Molecular Weight 141.21
Beilstein 20(3/4)1977
Reaxy-Rn 111506

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
E2430439 Certificate of Analysis Apr 16, 2024 T162332
E2430455 Certificate of Analysis Apr 16, 2024 T162332

Chemical and Physical Properties

Sensitivity Light Sensitive,Hygroscopic,Heat Sensitive
Boil Point(°C) 73 °C/1 mmHg
Melt Point(°C) 61 °C
Molecular Weight 141.210 g/mol
XLogP3 0.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 0
Exact Mass 141.115 Da
Monoisotopic Mass 141.115 Da
Topological Polar Surface Area 28.800 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 180.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Yang Zhao, Biao Ma, Xiaomei Liu, Ning Li, Yang Li, Xiaobin Fan, Wenchao Peng.  (2023)  Microwave and template assisted synthesis of atomically dispersed Co–N2 sites on carbon spheres for Fenton-like reaction.  CARBON,  214  (118371). 

Solution Calculators

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