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N-Methylsuccinimide - >98.0%(GC), high purity , CAS No.1121-07-9

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N-Methylsuccinimide - >98.0%(GC), high purity , CAS No.1121-07-9

1 Citations

COA

Grade & Purity:

≥98%(GC)

Cas Number: 1121-07-9
Molecular Weight: 113.12
MDL number: MFCD00005517
PubChem CID: 70717
PubChem SID: 488184576

In stock

Item Number

N159128

Grouped product items
SKU	Size	Availability	Price
N159128-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$10.90
N159128-5g	5g	1	$41.90
N159128-10g	10g	2	$75.90
N159128-25g	25g	3	$112.90
N159128-100g	100g	1	$403.90

View related series

Carbonyl compound (2335) Imide (271)

Basic Description

Synonyms	D70368 \| Hydrogen gas \| SCHEMBL27941 \| (+-)-Homocysteine \| DTXSID40149902 \| EN300-211529 \| N-METHYL SUCCINIMIDE \| AC-15701 \| MFCD00005517 \| InChI=1/C5H7NO2/c1-6-4(7)2-3-5(6)8/h2-3H2,1H \| 1-Methyl-2,5-pyrrolidinedione \| UNII-FT9GT286W2 \| Succinimide, N-met
Specifications & Purity	≥98%(GC)
Shipped In	Normal
Product Description	N-Methylsuccinimide is a metabolite of N-methyl-2-pyrrolidone (NMP) and its presence in in plasma and urine can be used as a biomarker of exposure to NMP. Hydrogen bonded complexes between N-methylsuccinimide and phenols (pKa = 10.2 → 6) are investigated by infrared spectrometry. N-Methylsuccinimide was employed as model compound to investigate the mechanism of enolization step by density-functional theory (DFT) calculations

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Carboxylic acid derivatives
      - Level5 Carboxylic acid imides
        Level6 N-substituted carboxylic acid imides

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Carboxylic acid derivatives
Intermediate Tree Nodes	Carboxylic acid imides
Direct Parent	N-substituted carboxylic acid imides
Alternative Parents	Pyrrolidine-2-ones N-alkylpyrrolidines Dicarboximides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Carboxylic acid imide, n-substituted - Pyrrolidone - 2-pyrrolidone - N-alkylpyrrolidine - Dicarboximide - Pyrrolidine - Lactam - Azacycle - Organoheterocyclic compound - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as n-substituted carboxylic acid imides. These are compounds comprising an N-substituted carboxylic acid imide group, with the general structure R1N(C(R2)=O)C(R3)=O (R2,R3=H, alkyl, aryl; R1=Anything but H).
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

Mechanisms of Action

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

Names and Identifiers

Pubchem Sid	488184576
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184576
IUPAC Name	1-methylpyrrolidine-2,5-dione
INCHI	InChI=1S/C5H7NO2/c1-6-4(7)2-3-5(6)8/h2-3H2,1H3
InChIKey	KYEACNNYFNZCST-UHFFFAOYSA-N
Smiles	CN1C(=O)CCC1=O
Isomeric SMILES	CN1C(=O)CCC1=O
WGK Germany	2
RTECS	UY1028650
Molecular Weight	113.12
Reaxy-Rn	110534
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=110534&ln=

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.

13 results found

Lot Number	Certificate Type	Date	Item
E1913049	Certificate of Analysis	Mar 08, 2023	N159128
G23051262	Certificate of Analysis	Feb 10, 2023	N159128
G23051270	Certificate of Analysis	Feb 10, 2023	N159128
G23051267	Certificate of Analysis	Feb 10, 2023	N159128
G23051263	Certificate of Analysis	Feb 10, 2023	N159128
G23051266	Certificate of Analysis	Feb 10, 2023	N159128
G2405011	Certificate of Analysis	Feb 10, 2023	N159128
G23051265	Certificate of Analysis	Feb 10, 2023	N159128
G23051268	Certificate of Analysis	Feb 10, 2023	N159128
G23051269	Certificate of Analysis	Feb 10, 2023	N159128
A2224200	Certificate of Analysis	Dec 16, 2021	N159128
A2224374	Certificate of Analysis	Dec 16, 2021	N159128
A2224376	Certificate of Analysis	Dec 16, 2021	N159128

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Chemical and Physical Properties

Solubility	Soluble in methanol
Sensitivity	Moisture sensitive
Boil Point(°C)	235°C
Melt Point(°C)	70 °C
Molecular Weight	113.110 g/mol
XLogP3	-0.900
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	113.048 Da
Monoisotopic Mass	113.048 Da
Topological Polar Surface Area	37.400 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	125.000
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

How to Cite Aladdin Scientific Products?

1. Xianliang Qiao, Xinyu Liu, Yang Yang, Zhenhua Mao, Tianhe Li, Lele Gao, Chaoyue Zhao, Qingxin Guan, Wei Li. (2022) Carbon-Supported Au Catalyst in Acetylene Hydrochlorination: Enhancing Catalytic Performance by Complexation of Dicarbonyl Ligands. ChemCatChem, 14 (21): (e202200785).

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