N-Methylpyrrolidone
Based on 1 publication(s) in Google Scholar
N-Methylpyrrolidone (1-Methyl-2-pyrrolidinone), a five-membered cyclic amide, is an orally active organic polar solvent with teratogenicity and toxicity. N-Methylpyrrolidone is low in acute toxicity with a LD50 value of 3914 mg/kg in rats and of 4050 mg/kg in mice. N-Methylpyrrolidone is extensively used in the manufacture of adhesives, paints, fuels, and pharmaceuticals.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- Purity : 99.99%
- CAS No.: 872-50-4
- 화학식: C5H9NO
- 분자량:99.13
-
보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
Biological Activity
-
Chemical Information
-
용액&용해도
- Protocol
- 순도&문서
- References
-
Help & FAQs
-
HY-Y0320
Dimethyl sulfoxide, meets analytical specification of Ch.P.Aprotic Solvent -
HY-Y1893
Solutol HS-15 -
HY-W042416
N,N-DimethylacetamideAnti-inflammatory agent -
HY-Y0873A
PEG400 -
HY-Y0320C
Dimethyl sulfoxideAprotic Solvent -
HY-Y0873
PEG300Neutral Polymer -
HY-Y0320D
Dimethyl sulfoxide, cryoprotectant vitrification agentBiochemical Assay Reagent -
HY-Y0320R
Dimethyl sulfoxide (Standard)Aprotic Solvent -
HY-Y0320GL
Dimethyl sulfoxide (GMP Like)GMP Like class DMSO -
HY-17031
SBE-β-CDExcipient
Publications Citing Use of MedChemExpress (MCE) N-Methylpyrrolidone
More
Biological Activity
제품 설명
In Vitro
N-Methylpyrrolidone (5.0 mM, 11 h) is removed by NJUST38 with the supplementation of nitrate into anoxic system[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:Rats[3]
-
Dosage:0-30000 ppm
-
Administration:feed, daily for 28 days
-
Result:Showed hematological (mild to moderate leukopenia) and histopathological alterations (hypocellular bone marrow, testicular degeneration and atrophy, and thymic atrophy), and cloudy swelling of the epithelia of the distal parts of the renal tubuli in mice.
Clinical Trial
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
-
CAS No. 872-50-4
-
Appearance Liquid (Density: 1.03 g/mL)
-
분자량 99.13
-
화학식 C5H9NO
-
Color Colorless to light yellow
-
SMILES
O=C1N(C)CCC1
-
Synonyms
NMP; 1-Methyl-2-pyrrolidinone
-
선적
Room temperature in continental US; may vary elsewhere.
-
보관
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
-
Journal Impact Factor
-
Most Recent
용액&용해도
In Vitro:
DMSO : 100 mg/mL (1008.78 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Protocol
-
Reproductive and Developmental Toxicity Study
Reproductive and developmental toxicity studies detect adverse effects of prenatal or peri/postnatal exposure on maternal condition, pregnancy maintenance, embryo-fetal survival, fetal growth, structural development, and offspring reproductive or developmental endpoints; classic rat protocols generate readouts by comparing treated groups with vehicle, pair-fed, or untreated controls for implantation, resorption, fetal weight, crown-rump length, external morphology, visceral morphology, skeletal ossification, anogenital distance, nipple/areola retention, and postnatal cohort outcomes.
-
Acute Systemic Toxicity Study
Acute systemic toxicity studies evaluate adverse effects occurring after a single exposure, or repeated exposure within a short acute window, and the main in vivo readouts are mortality, moribund condition, clinical signs, body-weight change, and gross pathological findings; acute oral toxicity methods were developed to replace classical LD50 testing with reduced-animal designs such as fixed-dose procedure, acute toxic class method, and up-and-down procedure. The fixed-dose procedure classifies acute toxicity by administering predefined dose levels and observing evident toxicity rather than using death as the primary endpoint, whereas the acute toxic class method uses sequential groups of three animals per step and the up-and-down procedure doses animals sequentially to estimate an LD50 with fewer animals than conventional LD50 testing.
순도&문서
-
Data Sheet (295 KB)
-
SDS (560 KB)
- English - EN (560 KB)
- Français - FR (560 KB)
- Deutsch - DE (560 KB)
- Norwegian - NO (560 KB)
- Español - ES (560 KB)
- Swedish - SV (560 KB)
- Italian - IT (560 KB)
- Korean - KR (560 KB)
- Portuguese - PT (560 KB)
-
Handling Instructions (2659 KB)
References
[1]. Jing Wang, et al. Nitrate stimulation of N-Methylpyrrolidone biodegradation by Paracoccus pantotrophus: Metabolite mechanism and Genomic characterization. Bioresour Technol. 2019 Dec;294:122185. [Content Brief]
[2]. Claudia Julieta Solís-González, et al. Novel Metabolic Pathway for N-Methylpyrrolidone Degradation in Alicycliphilus sp. Strain BQ1. Appl Environ Microbiol. 2017 Dec 15;84(1):e02136-17. [Content Brief]
[3]. Malek DE, et al. Repeated dose toxicity study (28 days) in rats and mice with N-methylpyrrolidone (NMP). Drug Chem Toxicol. 1997 Feb-May;20(1-2):63-77. [Content Brief]
[4]. Malley LA, et al. 90-day subchronic toxicity study in rats and mice fed N-methylpyrrolidone (NMP) including neurotoxicity evaluation in rats. Drug Chem Toxicol. 1999 Aug;22(3):455-80. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Complete Stock Solution Preparation Table
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 10.0878 mL | 50.4388 mL | 100.8776 mL | 252.1941 mL |
| 5 mM | 2.0176 mL | 10.0878 mL | 20.1755 mL | 50.4388 mL | |
| 10 mM | 1.0088 mL | 5.0439 mL | 10.0878 mL | 25.2194 mL | |
| 15 mM | 0.6725 mL | 3.3626 mL | 6.7252 mL | 16.8129 mL | |
| 20 mM | 0.5044 mL | 2.5219 mL | 5.0439 mL | 12.6097 mL | |
| 25 mM | 0.4035 mL | 2.0176 mL | 4.0351 mL | 10.0878 mL | |
| 30 mM | 0.3363 mL | 1.6813 mL | 3.3626 mL | 8.4065 mL | |
| 40 mM | 0.2522 mL | 1.2610 mL | 2.5219 mL | 6.3049 mL | |
| 50 mM | 0.2018 mL | 1.0088 mL | 2.0176 mL | 5.0439 mL | |
| 60 mM | 0.1681 mL | 0.8406 mL | 1.6813 mL | 4.2032 mL | |
| 80 mM | 0.1261 mL | 0.6305 mL | 1.2610 mL | 3.1524 mL | |
| 100 mM | 0.1009 mL | 0.5044 mL | 1.0088 mL | 2.5219 mL |
N-Methylpyrrolidone Related Classifications
HY-Y1275 Related Classifications
Powered by Bioz