Does BMA mean n-butyl methacrylate or isobutyl methacrylate?

In most commercial usage the bare abbreviation means the normal isomer, n-butyl methacrylate, CAS 97-88-1. The branched isomer, isobutyl methacrylate, is a different substance with its own identifiers and a different contribution to copolymer hardness, and the tertiary isomer is different again. Because all three are abbreviated loosely in day-to-day correspondence, an order written as BMA alone is ambiguous. Write the full chemical name and the CAS number on every enquiry, purchase order and goods-inwards record.

Why must the monomer not be blanketed with pure nitrogen?

Because the stabiliser used in commercial methacrylate monomers requires dissolved oxygen to function. It intercepts radicals by a mechanism that consumes oxygen, so a drum stripped of oxygen contains an inhibitor that is chemically present and functionally absent. The correct headspace is air, or air diluted with nitrogen to a specified oxygen content, never an inert blanket. This is one of the very few cases in a chemical store where displacing oxygen makes a material more dangerous rather than less, and it catches people whose instinct is trained on flammable solvents.

How should inhibitor content be read on a certificate?

As a starting condition rather than a permanent property. The certificate reports the inhibitor level at release; that level falls in storage as the stabiliser does its job, and it falls faster in warm conditions, in light and in the presence of contamination. A long-stored drum can meet its original certificate on every other line while having very little inhibitor left. Where storage has been long or uncertain, retest the inhibitor level before charging a reactor rather than relying on the release figure.

What is popcorn polymerisation and why does it matter here?

It is a self-propagating, expanding polymer growth that forms in dead legs, vapour spaces, valve bonnets and residues where inhibitor cannot reach. Once seeded it continues under conditions that would not start a normal polymerisation, and it grows mechanically enough to jam valves and distort equipment. The controls are housekeeping controls: no unswept dead legs, no long-standing residues, no lines left full between campaigns, and clean vessels before refilling. It is not a reason to avoid methacrylate monomers, but it is a reason to design the pipework as if the monomer were reactive, because it is.

How does the butyl ester change a copolymer compared with the methyl one?

The four-carbon ester side chain is flexible and bulky, so it loosens chain packing and lowers the temperature at which the polymer softens. Against the methyl ester it gives a softer, more flexible and more extensible polymer, better adhesion and easier film formation, at the cost of hardness and block resistance. Against the corresponding acrylate it gives a harder polymer with the weathering advantage of the methacrylate backbone. Formulators use it as the soft component of an all-methacrylate system, which keeps the durability while tuning flexibility.

Co to jest N-Methylformamide?

N-Methylformamide to związek chemiczny zarejestrowany pod numerem CAS 123-39-7. Wzór sumaryczny: C2H5NO. Masa molowa: 59.07 g/mol. IUPAC: N-methylformamide.

Jaki jest numer CAS N-Methylformamide?

Numer CAS dla N-Methylformamide to 123-39-7 — unikalny identyfikator Chemical Abstracts Service (CAS).

Jaki jest wzór sumaryczny N-Methylformamide?

Wzór sumaryczny: C2H5NO. Masa molowa: 59.07 g/mol. logP (XLogP3): -1. PSA: 29.1 Å².

Jakie są zagrożenia N-Methylformamide według GHS?

Według klasyfikacji GHS N-Methylformamide wymaga oznaczenia zwrotami zagrożenia: H360D (Może działać szkodliwie na dziecko w łonie matki), H312 (Działa szkodliwie w kontakcie ze skórą).

Gdzie można kupić N-Methylformamide?

N-Methylformamide jest dostępny w naszym sklepie. Zobacz produkt: https://epchems.online/products/n-methylformamide/

Skąd pochodzą dane chemiczne dla N-Methylformamide?

Dane chemiczne dla N-Methylformamide pochodzą z autorytatywnych źródeł: PubChem (NIH), ChEMBL (EBI). PubChem CID: 31254. Zgodne z Rozporządzeniem CLP (WE 1272/2008), dostępne na licencji CC-BY 4.0.

N-Methylformamide

CAS 123-39-7 · C₂H₅NO · MW 59.07 g/mol

O związku N-Methylformamide

N-Methylformamide to związek chemiczny zarejestrowany pod numerem CAS 123-39-7 o wzorze sumarycznym C₂H₅NO i masie molowej 59.07 g/mol.

Cząsteczka zawiera 9 atomów połączonych 8 wiązaniami chemicznymi. Pełna nazwa systematyczna IUPAC dla tego związku to N-methylformamide. Powyższy interaktywny model 3D pozwala obejrzeć układ przestrzenny atomów — można go obracać myszką, powiększać scrollem oraz przełączać między trybami wizualizacji szkieletowy / Ball & Stick / Space Fill.

Pod względem właściwości fizykochemicznych współczynnik podziału logP = -1 (wartość ujemna, związek hydrofilowy), powierzchnia polarna PSA = 29.1 Å², 1 donorów i 1 akceptorów wiązań wodorowych. Te parametry są kluczowe przy ocenie biodostępności i interakcji z biomolekułami.

Dane chemiczne dla tego związku pochodzą z PubChem (NIH NLM NCBI), jednej z największych baz związków chemicznych na świecie. Wszystkie informacje są aktualizowane automatycznie i wzbogacone o tłumaczenia zwrotów GHS zgodne z Rozporządzeniem CLP (1272/2008/WE). Powyższy widget można używać do celów edukacyjnych, badawczych i komercyjnych.

Właściwości fizykochemiczne

Wzór sumaryczny	C₂H₅NO
Masa molowa	59.07 g/mol
IUPAC	N-methylformamide
SMILES	`CNC=O`
InChIKey	`ATHHXGZTWNVVOU-UHFFFAOYSA-N`
logP (XLogP3)	-1
PSA	29.1 Å²
HBD / HBA	1 / 1
PubChem CID	CID 31254 ↗

Bezpieczeństwo GHS

Sygnał: Niebezpieczeństwo

GHS07

GHS08

? — H360D

H312 — Działa szkodliwie w kontakcie ze skórą

Literatura naukowa

20 artykułów · 12 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (20 artykułów)

Wysokość słupka = liczba artykułów w roku. Hover dla szczegółów.

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Thermodynamic Study of N-Methylformamide and N,N-Dimethyl-Formamide.

Růžička K, Štejfa V, Červinka C et al. (2024) · Molecules (Basel, Switzerland)

Cytowania: 5Open AccessDOI ↗PubMed ↗PDF ↗

How water links to cis and trans peptidic groups: the rotational spectrum of N-methylformamide-water.

et al. (2010)

Cytowania: 31$ PaywallDOI ↗PubMed ↗

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Carbonyl stretching band in amides as Lorentz oscillator. Insights into anharmonicity and local environment in the liquid phase from NIR and MIR spectra of N-methylformamide and di-N,N-methylformamide.

et al. (2025)

Cytowania: 4Open AccessDOI ↗PubMed ↗PDF ↗

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Use of N-methylformamide as a solvent in indium-promoted Barbier reactions en route to enediyne and epoxy diyne formation: comparison of rate and stereoselectivity in C-C bond-forming reactions with water.

et al. (2009)

Cytowania: 7Open AccessDOI ↗PubMed ↗PDF ↗

Photo-stability of peptide-bond aggregates: N-methylformamide dimers.

et al. (2014)

Cytowania: 15$ PaywallDOI ↗PubMed ↗

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Interfacial Structure and Interaction of Kaolinite Intercalated with N-methylformamide Insight from Molecular Dynamics Modeling.

et al. (2018)

Cytowania: 6Open AccessDOI ↗PubMed ↗PDF ↗

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One-Step, One-Lane Chemical DNA Sequencing by N-Methylformamide in the Presence of Metal Ions

Rodolfo Negri, Giovanna Costanzo, Raffaele Saladino et al. (1996) · BioTechniques

Cytowania: 26Open AccessDOI ↗PDF ↗

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Effects of urea on the aqueous solvation structure and dynamics of cis/trans-N-methylformamide: An insight from molecular dynamics simulation study

Chinmay Parida, Pragin Chettiyankandy, Apramita Chand et al. (2024) · Chemical Physics Impact

Cytowania: 1Open AccessDOI ↗PDF ↗

CH stretching vibration of N-methylformamide as a sensitive probe of its complexation: infrared matrix isolation and computational study.

et al. (2011)

Cytowania: 7$ PaywallDOI ↗PubMed ↗

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Computational investigation of the gas-phase formation and spectroscopic analysis of cis-N-Methylformamide

Jerusha Singh Mahima, Mishra Pravi, Pandey Parmanand et al. (2026) · EPJ Web of Conferences

Open AccessDOI ↗PDF ↗

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Process optimization for suppressing N-methylformamide hydrolysis and methylamine generation in stripper solution

Jinjuan Ni, Huilai Liu, Dali Bao et al. (2026) · Desalination and Water Treatment

Open AccessDOI ↗PDF ↗

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Viscosities and thermodynamics of viscous flow of N-methylformamide/N-methylacetamide + polyethylene glycol 200/300/400 binary systems: Experimental and theoretical exploration

Anil Kumar Nain, Abhimanyu Nain (2026) · Chemical Thermodynamics and Thermal Analysis

Open AccessDOI ↗PDF ↗

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Vulnerable Factors Affecting Urinary N-Methylformamide Concentration among Migrant Workers in Manufacturing Industries in Comparison with Native Workers in the Republic of Korea (2012-2019).

et al. (2022)

Cytowania: 1Open AccessDOI ↗PubMed ↗PDF ↗

Spectroscopic and molecular modeling studies on the interactions of N-Methylformamide with superoxide dismutase.

et al. (2014)

Cytowania: 2$ PaywallDOI ↗PubMed ↗

Separation of chelating agents as copper complexes by capillary zone electrophoresis using quaternary ammonium bromides as additives in N-methylformamide.

et al. (2006)

Cytowania: 2$ PaywallDOI ↗PubMed ↗

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Local intermolecular structure, hydrogen bonding and related dynamics in the liquid cis/trans N-methylformamide mixture: A density functional theory based Born-Oppenheimer molecular dynamics study

Ioannis Skarmoutsos, Ricardo L. Mancera, Stefano Mossa et al. (2022) · arXiv (2209.01801v1)

Open AccessDOI ↗PDF ↗

Simultaneous determination of N-hydroxymethyl-N-methylformamide, N-methylformamide and N-acetyl-S-(N-methylcarbamoyl)cystein in urine samples from workers exposed to N,N-dimethylformamide by liquid chromatography-tandem mass spectrometry.

et al. (2005)

Cytowania: 6$ PaywallDOI ↗PubMed ↗

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Solid-liquid equilibria and excess enthalpies in binary mixtures of acetophenone with some aliphatic amides

Ana Cobos, Patryk Sikorski, Juan Antonio González et al. (2024) · arXiv (2409.12768v1)

Cytowania: 5Open AccessDOI ↗PDF ↗

Identification of potential genomic biomarkers of hepatotoxicity caused by reactive metabolites of N-methylformamide: Application of stable isotope labeled compounds in toxicogenomic studies.

et al. (2006)

Cytowania: 10$ PaywallDOI ↗PubMed ↗

A dual-emitting Tb(iii)&Yb(iii)-functionalized coordination polymer: a "turn-on" sensor for N-methylformamide in urine and a "turn-off" sensor for methylglyoxal in serum.

et al. (2019)

Cytowania: 8$ PaywallDOI ↗PubMed ↗

Dane z PubMed (NIH NLM), OpenAlex (CC0), Semantic Scholar (AI2). AI Summary wygenerowane przez Semantic Scholar TLDR. Artykuły z ikoną wymagają płatnego dostępu.

Synonimy

N-METHYLFORMAMIDE · 123-39-7 · Methylformamide · Formamide, N-methyl- · Monomethylformamide · N-Monomethylformamide · n-methyl-Formamide · NSC 3051 · EK 7011 · Formic acid amide, N-methyl- · X 188 · XPE4G7Y986 · NSC3051 · NSC-3051 · CHEBI:7438

Data sources

📊 PubChem CID 31254 — NIH
🔬 NIST WebBook — spektroskopia
🌐 Wikidata
💊 ChEMBL — bioaktywność

Kup w sklepie

N-Methylformamide →

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