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Isobutyraldehyde Basic informationes

Description References

Product nomen:	Isobutyraldehyde
CAS;	78-84-2
MF:	C4H8O
MW:	72.11
EINECS:	201-149-6
Categoria:	Carbonyl componit; Donec Synthesis, Aldehydes, aedificium cuneos, C1 ad C6, Organic Aedificium obstruit
Mol fasciculi:	78-84-2.

Isobutyraldehyde Chemical Properties

punctum liquescens	−65 °C(lit.)
fervens	63 °C(lit.)
density	0.79 g/mL at 25 °C(lit.)
vapor density	2.5 (vs. aere);
vapor pressura	66 mm Hg (4.4 °C)
FEMA	2220 \| ISOBUTYRALDEHYDE
refractivus index	n20/D 1.374(lit.)
Fp	−40 °F
repono temp.	2-8°C
solubility	aquam; soluble11g/100mL ad 20°C(lit.)
forma	Liquid
color	Patet
Odor	Ponticus.
odor Limen	0.00035ppm
explosive modum	1.6-11.0%(V)
Aqua Solubility	75 g/L (20 C)
Sensitiva	Air Sensitiva
JECFA Number	252
Merck	14,5154
BRN	605330
Stabilitas:	Stabulum. Refrigerandum. Magnopere fomes. Impugnabilia sunt agentibus validis oxidizing, basibus validis; fortis acida, fortis reducens.
CAS Reference	78-84-2 (CAS Reference)
NIST Chemia Reference	Propanal, 2-methyl-(78-84-2)
EPA Substantia Registry System	Isobutyraldehyde (78-84-2)

Isobutyraldehyde Safety Information

Periculum Codes	F, Xn, XI .
Periculum Denunciationes	11-22-36
Salus Denunciationes	16-36/37-9-33-29-26
RIDADR	UN 2045 3/PG 2
WGK Germania	1
RTECS	NQ4025000
F	9-13-23
Autoignition Temperature	91 °F
TSCA	Ita
HS Code	2912 19 00
HazardClass	3
PackingGroup	II
Ancipitia substantiae Data	78-84-2
Toxicity	LD50 viva voce in muribus: 3.7 g/kg (Smyth)

Isobutyraldehyde Ritus et Synthesis

Descriptio	Isobutyraldehyde, etiam ut 2-Methylpropanal, est compositio organica quae domus aldehydes, quae inveniuntur in alcoholicis potionibus, tea, panibus; suilla cocta, hastam oleum cum fructibus recentibus, ut pomum, fixa; cerasus, etc. Id conficitur per hydroformylationem propene, plerumque adeptus est latus, opus. Applicari potest ut fons ad alium producendum oeconomiae, inter alcohole isobutyl, glycol neopentyl tum productio acidum isobutanoicum et amino acida producebat ut valine et leucine. Praeterea isobutyraldehyde vulgo inservit pro intermedio in agro eget industria fabricandi pharmaceuticals (ut Vitaminum B5), fructus tutelae seges, pesticides, resinae syntheticae; facilisis, vulcanisatio acceleratores, auxilia textilia, unguentaria et sapores.
References	https://pubchem.ncbi.nlm.nih.gov/compound/isobutyraldehyde#section=Top http://chemindustry.ru/Isobutyraldehyde.php http://product-finder.basf.com/group/corporate/ https://en.wikipedia.org/wiki/Isobutyraldehyde
Descriptio	Isobutyraldehyde est proprium odoris. Synthesized per oxidatio isobutyl alcohol cum potassae dichromatis et acidi sulphurici concentrati.
Chemical Properties	Isobutyraldehyde est proprium acrem, acri odore.
Chemical Properties	hyalina liquida cum maxime ingratus odor
Eventum	Nuntiavit in * pomum et aromata rorantia et in unguentis essentialibus ex foliis tabaci et tea folia, item in unguentis Pini Jeffreyi Murr essentialis. folia citri folia aurantium, et Datura stramonium. Nuntiata inventa sunt pomo, Musa; dulce et acerbum cerasium, currantem, kohlrabi, amet, apium, pisum, annuum; lycopersiciSusceptibility, peppermint frumentum, menta et hastam oleum, acetum, triticum et siligo panes, caseos, butyrum, yogurt, ovum, caviar, pisces pingue, carnes, oleum salit; cerevisia, sublimatum, -orum, sherry, cider, whiskies, uva vina, cocoa, capulus, tea; avellanae, arachidis, popcorn, avenae, soybeans, mel, fungos, macadamia, nuces; BRASSICA, pirum et pomum sublimatum, oryza, sukiyaki, malt, loquat, clary salvia; squillis, tuber, pectines et lolligo
usus	Isobutyraldehyde est cellulosa esters synthesisof usus est, resina et plasticizers, in praeparatio acidi pantothenici andvalini; et saporibus.
usus	In summa acidum pantothenicum, valinum, leucinum, cellulosum esters, unguenta, sapores, plastici resina, gasoline additiva.
Definition	Chebi: Sodalis genus propanals id est propanal substitutus yl coetus ad positus II.
Praeparatio	Per oxidatio of * alcohol isobutyl cum dichromate potassae et acido sulphurico contracto.
Aroma limina values	Deprehensio: 0,4 ad 43 ppb'
General Description	Patet hyalina liquorem acri odore. Flash point of -40°F. Minus densa quam aqua et insolubilis aqua. Hinc natat aqua. Vapores aere graviores sunt. Used " ut oeconomiae aliae.
Aer & aqua Reactiones	Magnopere fomes. Oxidizes lente aspirante aere. Firmum (minus quam X% compositione) for quattuor horis expositae luci et aere in ratio clausa. Firmum duos hebdomades sub nitrogene conditis ad temperaturae usque ad 77°F. Insolubilis in aquam.
Reactividad Profile	Isobutyraldehyde can fortiter agere cum reducendis agentibus, agentibus oxidizing, basibus validis et acida mineralia. Potest subire exothermic sui condensationem seu polymerization motus qui ab acido saepe catalyzed. Fomes generat et / vel toxicus vapores in compositione cum azo, composita diazo, dithiocarbamates, nitrides; et fortes procuratores minuentes. Tardius cum expositae aerem in aerem reflectitur da peroxides et alia producta. Hae motus a luce reducuntur; catalysed per salia metallorum transeuntium, et sunt autocatalytici (catalyzed by ) eorum producta). Additio stabilimenta (facilisis) retardat autoxidatio.
Discrimen	Valde fomes, periculosum incendii et explosionis periculum. Pellis oculosque irritat.
Periculum salutis	Vapor est vexo ad oculos et membranulas mucosae.
Periculum salutis	Isobutyraldehyde est mediocriter cutem eyeirritant; quod effectus potest esse leviter major of n-butyraldehyde. An amounttotaling D mg in XXIV horas produci severeskin irritatio in leporibus; 100 mg irritatio oculi effecit moderata. The toxicity of isobutyraldehyde determinatio testium animalium valde inferior. Exposureto 8000 ppm (23,600 mg/m3) pro 4 horis waslethal ad mures. Valor LD50, oralis (mures): 2810 mg/kg.
Ignis Discrimen	Ignis mores: Vapores aere graviores sunt et pervadunt aliquantum ad fontem of ignition and flash back. Fires are difficult to control ob facilitatem decimo tertio.
Chemical Reactivity	Reactividad cum aqua nulla reactio; Reactividad cum Materiis Communibus: Non motus; Stabilitas Per Transport: Stabulum; Agentia pro acidis et causticis: Not pertineret; Polymerization: Not pertinent; Inhibitor Polymerizationis: Not pertineant.
Carcinogenicity	Isobutyraldehyde est non mutagenic in variis modis S. typhimurii et noncarcinogenic in mures et mures.
Purificationis Methodi	Arida isobutyraldehyde cum CaSO4 et uti statim post distillationem sub NITROGENIUM quia magna difficultas oxidatio prohibendi. Purgari potest per ejus Acidum bisulfitum derivativum. [Beilstein 1 IV 3262.]
vastum Dispositione	Isobutyraldehyde est combustus est in chemicaincinerator afterburner andscrubber instructus.

Isobutyraldehyde Praeparatio Products Et Rudis Materiae

Praeparatio Products

1-Butanol-->2-Methyl-1-propanol--> acidum Isobutyricum-->Methyl methacrylate-->Butyraldehyde-->2,2-Dimethyl-1,3-propanediol-->Isobutyronitrile-->L-Valine-->3-(4-ISOPROPYLPHENYL)ISOBUTYRALDEHYDE-->3-Methyl-2-butanone-->L-Valine-->3-(4-ISOPROPYLPHENYL)ISOBUTYRALDEHYDE-->3-Methyl-2-butanone-->Rifapentine-->L-Valine-->3-(4-ISOPROPYLPHENYL)ISOBUTYRALDEHYDE-->3-Methyl-2-butanone-->Rifapentine sal-->DL-PANTOLACTON-->ALDICARB-OXIME-->Carbosulfan-->2,5-Dimethyl-2,4-hexadiene-->2-AMINO-3-METHYLBUTANENITRILE-->FENPROPIMORPH-- >2-ISOPROPYL-6-METHYL-4-PYRIMIDINOL-->D-(-)-PANTOLACTONE-->Isobutylamine-->3-Hydroxy-2,2-dimethylpropanal-->DL-Valine-->2-Methylbutyl 2-methylbutyrate-->1-CHLORO-2-METHYLPROPYL CHLOROFORMATE-->1-CHLORO-2-METHYL-1-PROPENE-->2,6-DIMETHYL-5-HEPTENALE-->N,N''-(isobutylidene) diurea-->GERANYL ISOBUTYRATE-->2,2,4-Trimethyl-1,3-pentanediolmono(2-methylpropanoate)->5-METHYL-3-HEXEN-2-ONE-->Neopentyl glycol monoester hydropivalicate

Rudis materiae

CARBON MONOXIDE-->Potassium dichromate-->2-Methyl-1-propanol--> PROPYLENE-->BONYRAldehyde-->2-Amino-3-chlorobenzoicum acidum

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