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.

L-Lysine ist eine chemische Verbindung, registriert unter der CAS-Nummer 56-87-1. Summenformel: C6H14N2O2. Molmasse: 146.19 g/mol. IUPAC: (2S)-2,6-diaminohexanoic acid.

Wie lautet die CAS-Nummer von L-Lysine?

Die CAS-Nummer von L-Lysine ist 56-87-1 — eine eindeutige Kennung des Chemical Abstracts Service (CAS).

Wie lautet die Summenformel von L-Lysine?

Summenformel: C6H14N2O2. Molmasse: 146.19 g/mol. logP (XLogP3): -3. PSA: 89.3 Å².

Wo kann ich L-Lysine kaufen?

L-Lysine ist in unserem Shop erhältlich. Produkt ansehen: https://epchems.online/products/l-lysine/

Woher stammen die chemischen Daten für L-Lysine?

Die chemischen Daten für L-Lysine stammen aus zuverlässigen Quellen: PubChem (NIH), ChEMBL (EBI). PubChem CID: 5962. Konform mit der CLP-Verordnung (EG 1272/2008), verfügbar unter der Lizenz CC-BY 4.0.

L-Lysine

CAS 56-87-1 · C₆H₁₄N₂O₂ · MW 146.19 g/mol

Über L-Lysine

L-Lysine ist eine chemische Verbindung, registriert unter der Nummer CAS 56-87-1, mit der Summenformel C₆H₁₄N₂O₂, und einer Molmasse von 146.19 g/mol.

Das Molekül enthält 24 Atome, verbunden durch 23 chemische Bindungen. Der vollständige systematische IUPAC-Name dieser Verbindung lautet (2S)-2,6-diaminohexanoic acid. Das interaktive 3D-Modell oben zeigt die räumliche Anordnung der Atome — Sie können es mit der Maus drehen, mit dem Scrollrad zoomen und zwischen den Darstellungsmodi Skelett / Ball & Stick / Space Fill wechseln.

Hinsichtlich der physikalisch-chemischen Eigenschaften der Verteilungskoeffizient logP = -3 (negativer Wert, hydrophile Verbindung), polare Oberfläche PSA = 89.3 Å², 3 Donatoren und 4 Wasserstoffbrücken-Akzeptoren. Diese Parameter sind entscheidend für die Beurteilung der Bioverfügbarkeit und der Wechselwirkung mit Biomolekülen.

Die chemischen Daten für diese Verbindung stammen aus PubChem (NIH NLM NCBI), einer der größten chemischen Datenbanken der Welt. Alle Informationen werden automatisch aktualisiert und um GHS-Gefahrenhinweise gemäß der CLP-Verordnung (EG 1272/2008) ergänzt. Das obige Widget darf für Bildungs-, Forschungs- und kommerzielle Zwecke verwendet werden.

Physikalisch-chemische Eigenschaften

Wzór sumaryczny	C₆H₁₄N₂O₂
Masa molowa	146.19 g/mol
IUPAC	(2S)-2,6-diaminohexanoic acid
SMILES	`C(CCN)C[C@@H](C(=O)O)N`
InChIKey	`KDXKERNSBIXSRK-YFKPBYRVSA-N`
logP (XLogP3)	-3
PSA	89.3 Å²
HBD / HBA	3 / 4
PubChem CID	CID 5962 ↗

Wissenschaftliche Literatur

Literatura naukowa

11 artykułów · 8 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (11 artykułów)

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

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Computational and experimental insights into the spectroscopy, electronic states, and molecular docking of (2S)-2,6-diaminohexanoic acid [DAHA].

et al. (2025)

Cytowania: 1Open AccessDOI ↗PubMed ↗PDF ↗

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Heat Capacities of L-Cysteine, L-Serine, L-Threonine, L-Lysine, and L-Methionine

Václav Pokorný, Vojtěch Štejfa, Jakub Havlín et al. (2023) · Molecules

Open AccessDOI ↗PDF ↗

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Identification and Cobamide Coenzyme-dependent Formation of 3,5-Diaminohexanoic Acid, an Intermediate in Lysine Fermentation

E E Dekker, H A Barker (1968) · Journal of Biological Chemistry

Cytowania: 26Open AccessDOI ↗PDF ↗

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CYLD-mediated lysine63 deubiquitination regulates synaptic transmission and autophagy to mitigate age-related sequelae.

Sotiriou A, Konstantinidis G, Tavernarakis N (2026) · Nature communications

Open AccessDOI ↗PubMed ↗PDF ↗

Lysine.

(2006)

Review$ PaywallPubMed ↗

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Lysine restriction attenuates obesity-related anxiety-like behaviors via increasing Oscillibacter ruminantium-mediated tryptophol regulation.

Zhao F, Wang J, Liang W et al. (2025) · Microbiome

Open AccessDOI ↗PubMed ↗PDF ↗

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ETV4 lysine 2-hydroxyisobutyrylation promotes intrahepatic cholangiocarcinoma progression by suppressing ferroptosis through TXNIP downregulation.

Wu J, Ma Y, Wang X et al. (2026) · Cancer letters

Open AccessDOI ↗PubMed ↗PDF ↗

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KDM3A catalyses the oxidation of acetyl-lysine to hydroxyacetyl-lysine on histone H3K9.

Belle R, Bukowski JP, Schiller R et al. (2026) · Nature chemistry

Open AccessDOI ↗PubMed ↗PDF ↗

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Lysine malonylation regulates human sperm motility.

Cheng Y, Tian Y, Chen H et al. (2026) · Communications biology

Open AccessDOI ↗PubMed ↗PDF ↗

Lysine (2,6-Diaminohexanoic Acid, H2l)

O. Yamauchi, A. Odani (2016) · IUPAC Standards Online

$ PaywallDOI ↗

ChemInform Abstract: ABSOLUTE CONFIGURATION OF 3,5‐DIAMINOHEXANOIC ACID FROM THE β‐LYSINE MUTASE REACTION

F. KUNZ, J. RETEY, D. ARIGONI et al. (1978) · Chemischer Informationsdienst

$ PaywallDOI ↗

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

Synonyme

L-lysine · lysine · 56-87-1 · lysine acid · h-Lys-oh · (S)-Lysine · Aminutrin · alpha-Lysine · (S)-2,6-Diaminohexanoic acid · L-lys · Lisina · Lysinum · (S)-alpha,epsilon-Diaminocaproic acid · LYS (IUPAC abbreviation) · L-2,6-Diaminocaproic acid

Datenquellen

📊 PubChem CID 5962 — NIH
🔬 NIST WebBook — spektroskopia
🌐 Wikidata
💊 ChEMBL — bioaktywność

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