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Product Name: |
Isobutyraldehyde |
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CAS: |
78-84-2 |
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MF: |
C4H8O |
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MW: |
72.11 |
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EINECS: |
201-149-6 |
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Product Categories: |
Composita carbonyl; Synthesis Donec; aldehydes; Cuneos edificium, c6 C1 est, obstruit edificium Jr. |
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Mol File: |
78-84-2.mol |
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Liquescens punctum |
â € LXV ° C (Litt.) |
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Ferveret |
LXIII ° C (Litt.) |
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density |
0.79 g / ml at25 ° C (Litt.) |
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vapor densitatem, |
2.5 (vs caeli) |
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vapor pressura |
LXVI mm Aggaei (4.4 ° C) |
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potenti |
MMCCXX | ISOBUTYRALDEHYDE |
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refractivam index |
n20 / D 1.374 (lit.) |
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Fp |
â € XL ° F |
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temp repono. |
2-8 ° F |
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solubility |
aqua: soluble11g / 100ml ad XX ° C (Litt.) |
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forma |
Liquid |
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color |
liquet |
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Odor |
Pungent. |
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Odor Limen |
0.00035ppm |
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terminus explosive |
1.6-11.0% (V) |
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aqua Solubility |
LXXV g / L (XX ºC) |
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sensitivo |
aeris sensitiva |
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Number JECFA |
252 |
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Merck Poland |
14,5154 |
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BRN |
605330 |
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Stabilitatem: |
Firmum. Refrigerate.Highly flammabilia. Repugnat oxidizing agentia fortis fortis bases fortis acida validas redigo agentia. |
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CAS DataBase Reference |
78-84-2 (CAS DataBase Reference) |
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Quaestiones NIST Reference |
Propanal, II-methyl- (78-84-2) |
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Ratio Subcriptio quod substantia EPA |
Isobutyraldehyde (78-84-2) |
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aleam Codes |
F, X, XI |
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risk Denunciationes |
11-22-36 |
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Denunciationes salutem |
16-36 / 37-9-33-29-26 |
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RIDADR |
III IR MMXLV / PG II |
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Germania WGK |
1 |
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RTECS |
NQ4025000 |
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F |
9-13-23 |
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Autoignition Temperature |
CCCLXXXIV ° F |
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Capparis |
Ita |
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HS Code |
XIX 00 MMCMXII |
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HazardClass |
3 |
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PackingGroup |
II |
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Ancipitia substantiae Data |
78-84-2 (Malo Periculosam substantias Indicium) |
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Aedes |
LD50 viva apud mures inclusi essent: 3.7 g / kg (Smyth) |
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Description |
Isobutyraldehyde, also known as II-Methylpropanal, est organicum compositis ad thefamily de aldehydes, quae potest inveniri in bibitor potiones, tea, panis, cocta suilla, spearmint oleum tum nova fruges, ut pupillam, Musa sapientum fixa, cerasus; Factum est autem propene fabrica per hydroformylation etc., quasi inde-usuallyobtained opus. Potest applicari potest in producendo otherchemicals ad fontem, inter isobutyl alcohole crystallina specie neopentyl glycol, et quoque productio asisobutanoic Acidum amino acida ad producendum ut valineand leucine. Praeter, cui quidem ad medium fere isobutyraldehyde chemical industria agro ad attrahunt exercendis armorum officinis Specifar (ut asVitamin B5) seges praesidio products, pesticides, synthetica resins, facilisis, vulcanisation accelerators: textiles reliquorum auxiliorum pigmentaria andflavors. |
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Greek New |
https://pubchem.ncbi.nlm.nih.gov/compound/isobutyraldehyde#section=Top |
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Description |
Isobutyraldehyde hasa ratione odoris suavissimi componendum. Oxidatio de via summatim perstringitur isobutyl Vocatus acidum SULPHURATUS withpotassium dichromate conuenere. |
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Properties eget |
Isobutyraldehyde hasa naturam acri, effundens odorem proprium. |
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Properties eget |
maxime est colore cocta tetrum odorem spirant liquidwith |
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res |
Et nuntiavit inventus inapple RIBES odore ex tobacco foliis et essentialis olea andtea foliis, et in essentialis olea et pinus jeffreyi Murr. foliis Citrusaurantium foliis Datura stramonium. Referuntur in malo Musa dulcem et acidum cerasis currants, kohlrabi amet, apium, fabam, potatoes, consectetur peppermint frumentum monetae spearmint oleum, triticum ryebreads, caseorum, butyrum, ovi Caviar, fatty piscis, aletur cibis patris saliunt oleum, cerevisia sublimatum, nonnulla sherry, cider, whiskeys, uva vina, Tmolius Cocos, capulus, tea, apioque lustrasset, peanuts, popcorn, avena, soybeans, mel, fungos, macadamia nuces, BRASSICA, pirum et Apple sublimatum, rice, sukiyaki, brasii, loquat, sclareiam extinguere, squillis, tuber, pectines et echinos lolligo |
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usibus |
Nequando rapiat in cellulosa Isobutyraldehyde synthesisof esters, resinam et plasticizers in thepreparation andvaline pantothenic acidum est; et CAELESTI. |
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usibus |
Ofpantothenic acidum synthesis in, valine, leucine, Cellulose esters alii atque odores, sapores, plasticizers, dilutum resinam gasoline additives. |
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definitio |
ChEBI: A genus of the membrum propanals de loco hoc est propanal per yl atposition coetus II. |
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Praeparatio |
SULPHURATUS acidum oxidatio ofisobutyl per ipsum et potassium dichromate conuenere. |
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Aroma limine values |
DEPREHENSIO: 0.4 ad 43ppb |
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Communia |
A patet colorlessliquid et effundens odorem proprium. Mico punctum -40 ° F. Andinsoluble aqua rarior aqua. Hinc aquae supernatet. Vapores omnia graviora sunt caeli. Usedto et aliis chemicals. |
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Agrippina Minor aqua Aeris & |
Flammable.Oxidizes aer tardius aspirante gratia. Firmum (corrumpitur minus quam X%) forfour horis et cum lux caeli apud patere clausa ratio. Firmum in twoweeks cum NITROGENIUM stored sub temperaturis usque ad LXXVII Nubila. Inwater posse dissolvi. |
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Reactividad Profile |
Reducendo Isobutyraldehyde canreact intente procuratores et actores oxidizing fortis basesand acida mineralia. Contingit exothermic auto-densitate descendit, vel qui saepe polymerizationreactions catalyzed per acidum. Generat flammabiles et / vel toxicgases tandem coniunctim afficient vniuersa in Azo, Diazo componit, dithiocarbamates, nitrides et fortis reducing agentibus. Postquam patere caeli et aeris lente Reacts togive peroxides et alia products. Haec autem omnia operatur lucis aperiunt, catalyzed ab hiis quevis dubietas sales metallorum et non autocatalytic (catalyzed telorum portationibus products). Quod etiam ex stabilimenta (facilisis) retardsautoxidation. |
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aleam |
Fomes maxime periculosam explosione ignis periculum. Oculosque cutis irritationem. |
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salutem DISCRIMEN |
Irritatingto vapor oculis membranae mucosae. |
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salutem DISCRIMEN |
Et xiv Isobutyraldehyde modico cutis eyeirritant; quod effectus sit major leviter thatof butyraldehyde, n. An amounttotaling in D mg forma XXIV horas productum severeskinirritation cuniculosae Celtiberiae, C mg forma causedmoderate oculus offensis. |
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ignis DISCRIMEN |
Moribus igni vaporibus aere pauco interuallo Transite ad ignitionem sourceof facies et retro. Difficile est Saul ut purgaret ventrem ofreignition control debita ignes. |
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eget Reactividad |
Reactividad withWater nulla reactionem; Reactividad cum Clementine_Vulgate Materias: nullus motus; StabilityDuring Onerariis: Stabull; Acidis propter se curat ut medicamentis agens: Notpertinent; Polimerización: non pertinent; Matrix Polimerización: Notpertinent. |
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carcinogenicity |
Isobutyraldehyde isnot mutagenic in variis modos psalmum secum S. typhimurium et noncarcinogenic inrats et mures inclusi essent. |
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Ratio purificatione |
Et ita statim post distillatoria versatissimus CaSO4 isobutyraldehydewith excoquatur utor NITROGENIUM becauseof in magna difficultate in ne oxidatio. Potest purgabitur inde bisulfite throughits acidum. [I Beilstein 3262. iv] |
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Vastum dispositioni |
Isobutyraldehyde isburned in chemicalincinerator instructus cum afterburner andscrubber. |
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Praeparatio Products |
I-butanol -> Methyl, I-II, propanol -> Isobutyric acidum -> methyl methacrylate -> Butyraldehyde -> Dimethyl-2,2-1,3-propanediol -> Isobutyronitrile -> L. valine -> 3. (IV-ISOPROPYLPHENYL) ISOBUTYRALDEHYDE -> II-III-yl Butanona -> Rifapentine -> D - (+) - pantothenic acidum calcium sal -> Pantolactone-DL -> ALDICARB- OXIME -> Carbosulfan -> Dimethyl-2,5-2,4-hexadiene -> amino-II-III-METHYLBUTANENITRILE -> FENPROPIMORPH -> isopropyl-II-IV-VI-METHYL, PYRIMIDINOL -> D - (-) - PANTOLACTONE -> Isobutylamine -> Hydroxy-III-2,2-dimethylpropanal -> Valine-DL -> II-II-Methylbutyl methylbutyrate -> I-II-METHYLPROPYLCHLOROFORMATE-- chloro, > chloro, I-II, I-METHYL, propene -> Dimethyl-2,6-V-heptenal -> N, N '' - (isobutylidene) diurea -> GERANYL ISOBUTYRATE -> 2,2,4 -Trimethyl-1,3-pentanediolmono (methylpropanoate-II) -> METHYL-III-V-II, una-Hocus Pocus -> Neopentyl glycol monoesterhydropivalicate |
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et rudis materiae |
Carbo carbonis monoxide -> Kalium dichromate -> Methyl, I-II, propanol -> propylene -> Butyraldehyde -> II-III-Amino acid-chlorobenzoic |
