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.

Qu'est-ce que L-Valine ?

L-Valine est un composé chimique enregistré sous le numéro CAS 72-18-4. Formule brute: C5H11NO2. Masse molaire: 117.15 g/mol. IUPAC: (2S)-2-amino-3-methylbutanoic acid.

Quel est le numéro CAS de L-Valine ?

Le numéro CAS de L-Valine est 72-18-4 — un identifiant unique du Chemical Abstracts Service (CAS).

Quelle est la formule brute de L-Valine ?

Formule brute: C5H11NO2. Masse molaire: 117.15 g/mol. logP (XLogP3): -2.3. PSA: 63.3 Å².

Où acheter L-Valine ?

L-Valine est disponible dans notre boutique. Voir le produit : https://epchems.online/products/l-valine/

D'où proviennent les données chimiques de L-Valine ?

Les données chimiques de L-Valine proviennent de sources faisant autorité : PubChem (NIH), ChEMBL (EBI). PubChem CID: 6287. Conformes au règlement CLP (CE 1272/2008), disponibles sous licence CC-BY 4.0.

L-Valine

CAS 72-18-4 · C₅H₁₁NO₂ · MW 117.15 g/mol

À propos de L-Valine

L-Valine est un composé chimique enregistré sous le numéro CAS 72-18-4, de formule brute C₅H₁₁NO₂, et de masse molaire 117.15 g/mol.

La molécule contient 19 atomes reliés par 18 liaisons chimiques. Le nom systématique IUPAC complet de ce composé est (2S)-2-amino-3-methylbutanoic acid. Le modèle 3D interactif ci-dessus permet de visualiser l'arrangement spatial des atomes — vous pouvez le faire pivoter à la souris, zoomer avec la molette et basculer entre les modes de visualisation squelette / Ball & Stick / Space Fill.

Du point de vue des propriétés physico-chimiques, le coefficient de partage logP = -2.3 (valeur négative, composé hydrophile), surface polaire PSA = 63.3 Å², 2 donneurs et 3 accepteurs de liaisons hydrogène. Ces paramètres sont essentiels pour évaluer la biodisponibilité et l'interaction avec les biomolécules.

Les données chimiques de ce composé proviennent de PubChem (NIH NLM NCBI), l'une des plus grandes bases de données chimiques au monde. Toutes les informations sont mises à jour automatiquement et enrichies de traductions des mentions de danger GHS conformes au règlement CLP (CE 1272/2008). Le widget ci-dessus peut être utilisé à des fins éducatives, de recherche et commerciales.

Propriétés physico-chimiques

Wzór sumaryczny	C₅H₁₁NO₂
Masa molowa	117.15 g/mol
IUPAC	(2S)-2-amino-3-methylbutanoic acid
SMILES	`CC(C)[C@@H](C(=O)O)N`
InChIKey	`KZSNJWFQEVHDMF-BYPYZUCNSA-N`
logP (XLogP3)	-2.3
PSA	63.3 Å²
HBD / HBA	2 / 3
PubChem CID	CID 6287 ↗

Littérature scientifique

Literatura naukowa

10 artykułów · 2 open access · Źródła: PubMed, OpenAlex, Semantic Scholar

📈 Timeline publikacji (10 artykułów)

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

Thermodynamic Study of Some Amino Acids, 2-Aminopropanoic Acid, 2-Amino-3-methylbutanoic Acid, 2-Amino-4-methylpentanoic Acid, and 2-Amino-3-phenylpropanoic Acid in Aqueous Saccharide Solutions at Different Temperatures: Volumetric and Ultrasonic Study

Amalendu Pal, Nalin Chauhan (2011) · Journal of Chemical & Engineering Data

Cytowania: 41$ PaywallDOI ↗

Volumetric and Conductometric Behavior at T = 298.15 K of 2-[(2-Aminoacetyl)amino]acetic Acid, 2-[(2-Aminoacetyl)amino]-3-methylbutanoic Acid, and (2S)-2-[(2-Aminoacetyl)amino]-4-methylpentanoic Acid with Sodium Hexanoate

Zhenning Yan, Yang Zhao, Ronghua Xing et al. (2009) · Journal of Chemical & Engineering Data

Cytowania: 13$ PaywallDOI ↗

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(S,S)-2-(((Hydroxynaphth-1-yl)(4′-nitrophenyl)methyl)amino)-3-methylbutanoic Acid Methyl Ester

Maria Annunziata M. Capozzi, Cosimo Cardellicchio (2022) · Molbank

Cytowania: 3Open AccessDOI ↗PDF ↗

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SimpleDesign: A Joint Model for Protein Sequence and Structure Codesign

Jiarui Lu, Yuyang Wang, Yizhe Zhang et al. (2026) · arXiv (2609.03377v1)

Open AccessPDF ↗

( R )‐2‐Amino‐3‐mercapto‐3‐methylbutanoic Acid

Boheng Guan, Xuyu Liu (2026) · Encyclopedia of Reagents for Organic Synthesis

$ PaywallDOI ↗

2,4-Diamino-3-methylbutanoic acid, a novel amino acid in root nodule hydrolysates from Lotus tenuis

G.John Shaw, P.J. Ellingham, L.N. Nixon (1981) · Phytochemistry

Cytowania: 9$ PaywallDOI ↗

Coupling of [[922|ethyl (2S)‐2‐[(2S)‐2‐amino‐3‐phenylpropanamido]‐3‐phenylpropanoate trifluoroacetate salt]] with 2-naphthoxyacetic acid

Bart Dietrich (2020) · ChemSpider Synthetic Pages

$ PaywallDOI ↗

Diffusion coefficient of DL-2-amino-3-methylbutanoic acid in water

Jochen Winkelmann (2018) · Diffusion in Gases, Liquids and Electrolytes

$ PaywallDOI ↗

Crystal structure of leukotriene A4 hydrolase in complex with (2S)-2-amino-5-[[4-[(2S)-2-hydroxy-2-phenyl-ethoxy]phenyl]amino]-5-oxo-pentanoic acid

M.M.G.M. Thunnissen, M. Adler, M. Whitlow (2008) · Worldwide Protein Data Bank

$ PaywallDOI ↗

Crystal structure of ERAP2 aminopeptidase in complex with phosphinic pseudotripeptide((1R)-1-Amino-3-phenylpropyl){(2S)-3-[((2S)-1-amino-1-oxo-3-phenylpropan-2-yl)amino]-2-{[3-(2-hydroxyphenyl)-isoxazol-5-yl]methyl}-3-oxopropyl}phosphinic acid

P. Giastas, E. Stratikos, A. Mpakali (2022)

$ PaywallDOI ↗

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

Synonymes

L-valine · valine · 72-18-4 · (S)-Valine · (2S)-2-amino-3-methylbutanoic acid · (S)-2-Amino-3-methylbutanoic acid · 2-Amino-3-methylbutyric acid · (S)-2-Amino-3-methylbutyric acid · valina · L-alpha-Amino-beta-methylbutyric acid · L-valin · Valinum · (S)-alpha-Amino-beta-methylbutyric acid · NSC-76038 · l-(+)-alpha-Aminoisovaleric acid

Sources des données

📊 PubChem CID 6287 — NIH
🔬 NIST WebBook — spektroskopia
🌐 Wikidata
💊 ChEMBL — bioaktywność

Acheter en boutique

L-Valine →

Molécules apparentées

N-Butanol CAS 71-36-3 · C4H10O 1,2-Propylene Diacetate (PGDA) CAS 623-84-7 · C7H12O4 L-Serine CAS 56-45-1 · C3H7NO3 Vinyl acetate CAS 108-05-4 · C4H6O2 L-Lysine HCl CAS 657-27-2 · C₆H₁₅ClN₂O₂ Sodium Tripolyphosphate CAS 7758-29-4 · Na₅O₁₀P₃