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.

Che cos'è Formic Acid?

Formic Acid è un composto chimico registrato con il numero CAS 64-18-6. Formula bruta: CH2O2. Massa molare: 46.025 g/mol. IUPAC: formic acid.

Qual è il numero CAS di Formic Acid?

Il numero CAS di Formic Acid è 64-18-6 — un identificativo univoco del Chemical Abstracts Service (CAS).

Qual è la formula bruta di Formic Acid?

Formula bruta: CH2O2. Massa molare: 46.025 g/mol. logP (XLogP3): -0.2. PSA: 37.3 Å².

Quali sono i pericoli GHS di Formic Acid?

Secondo la classificazione GHS, Formic Acid deve riportare le seguenti indicazioni di pericolo: H226 (Liquido e vapori infiammabili.), H290 (Può essere corrosivo per i metalli.), H331 (Tossico se inalato.), H302 (Nocivo se ingerito.), H314 (Provoca gravi ustioni cutanee e gravi lesioni oculari.).

Dove acquistare Formic Acid?

Formic Acid è disponibile nel nostro negozio. Vedi il prodotto: https://epchems.online/products/formic-acid/

Da dove provengono i dati chimici di Formic Acid?

I dati chimici di Formic Acid provengono da fonti autorevoli: PubChem (NIH), ChEMBL (EBI). PubChem CID: 284. Conformi al Regolamento CLP (CE 1272/2008), disponibili con licenza CC-BY 4.0.

Formic Acid

CAS 64-18-6 · CH₂O₂ · MW 46.025 g/mol

Informazioni su Formic Acid

Formic Acid è un composto chimico registrato con il numero CAS 64-18-6, con formula bruta CH₂O₂, e massa molare di 46.025 g/mol.

La molecola contiene 5 atomi collegati da 4 legami chimici. Il nome sistematico IUPAC completo di questo composto è formic acid. Il modello 3D interattivo qui sopra permette di visualizzare la disposizione spaziale degli atomi — puoi ruotarlo con il mouse, zoomare con la rotellina e passare tra le modalità di visualizzazione scheletro / Ball & Stick / Space Fill.

Dal punto di vista delle proprietà chimico-fisiche, il coefficiente di ripartizione logP = -0.2 (valore negativo, composto idrofilo), superficie polare PSA = 37.3 Å², 1 donatori e 2 accettori di legami a idrogeno. Questi parametri sono fondamentali per valutare la biodisponibilità e l'interazione con le biomolecole.

I dati chimici di questo composto provengono da PubChem (NIH NLM NCBI), uno dei più grandi database chimici al mondo. Tutte le informazioni sono aggiornate automaticamente e arricchite con le traduzioni delle indicazioni di pericolo GHS conformi al Regolamento CLP (CE 1272/2008). Il widget qui sopra può essere utilizzato per scopi educativi, di ricerca e commerciali.

Proprietà chimico-fisiche

Wzór sumaryczny	CH₂O₂
Masa molowa	46.025 g/mol
IUPAC	formic acid
SMILES	`C(=O)O`
InChIKey	`BDAGIHXWWSANSR-UHFFFAOYSA-N`
logP (XLogP3)	-0.2
PSA	37.3 Å²
HBD / HBA	1 / 2
PubChem CID	CID 284 ↗

Sicurezza GHS

Sygnał: Niebezpieczeństwo

GHS02

GHS05

GHS06

GHS07

H226 — Łatwopalna ciecz i pary

H290 — Może powodować korozję metali

H331 — Działa toksycznie w następstwie wdychania

H302 — Działa szkodliwie po połknięciu

H314 — Powoduje poważne oparzenia skóry oraz uszkodzenia oczu

H318 — Powoduje poważne uszkodzenie oczu

Letteratura scientifica

Literatura naukowa

20 artykułów · 17 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (20 artykułów)

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

Update to RIFM fragrance ingredient safety assessment, formic acid, CAS Registry number 64-18-6.

Api AM, Belsito D, Botelho D et al. (2024) · Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association

$ PaywallDOI ↗PubMed ↗

🔓

Mechanisms of formic acid stress response in evolved yeast for microbial-electrocatalytic systems.

et al. (2026)