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Product Name: |
Isovaleraldehyde |
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Synonym: |
Bortezomib Impurity59, III, yl butyraldehyd: aldehydeisovalerianique; beta-Methylbutanal: Butanal,-2,2-III-hydroxy dimethyl-: Butanal, III, yl, Butanal, III-methyl-: Butyraldehyde, III-methyl- |
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CAS: |
590-86-3 |
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MF: |
C5H10O |
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MW: |
86.13 |
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EINECS: |
209-691-5 |
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Product Categories: |
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Mol File: |
590-86-3.mol |
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Liquescens punctum |
-60 ° C |
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Ferveret |
XC ° C (Litt.) |
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density |
0.803 g / ml at25 ° C (Litt.) |
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vapor densitatem, |
2.96 (vs caeli) |
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vapor pressura |
XXX mm Aggaei (XX ° C) |
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potenti |
MMDCXCII | III, METHYLBUTYRALDEHYDE |
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refractivam index |
n20 / D 1.388 (lit.) |
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Fp |
XXIX ° F |
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temp repono. |
Armarium frigidarium (IV + F) + area Flammables |
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solubility |
alcohol: miscible |
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forma |
Liquid |
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color |
Patet sine colore flavo tolight |
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terminus explosive |
1.7-6.8% (V) |
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Odor Limen |
0.0001ppm |
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aqua Solubility |
XV g / L (XX ºC) |
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Number JECFA |
258 |
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Merck Poland |
14,5229 |
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BRN |
773692 |
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Stabilitatem: |
Firmum et lightand caeli sensitivo. Altus flammabilia. Libenter forms explosive withair commixtionibus utebantur. Simul acri oxidizing agentibus bases redigo agentia auras. |
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InChIKey |
YGHRJJRRZDOVPD UHFFFAOYSA-N, |
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CAS DataBase Reference |
590-86-3 (CAS DataBase Reference) |
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Quaestiones NIST Reference |
Butanal, methyl--III (590-86-3) |
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Ratio Subcriptio quod substantia EPA |
Isovaleraldehyde (590-86-3) |
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aleam Codes |
F, XI |
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risk Denunciationes |
11-36-36 / XXXVII / 38-43-36 / XXXVII |
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Denunciationes salutem |
7-16-26-36-37 / 39-37-24-9 |
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RIDADR |
III IR MCMLXXXIX / PG II |
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Germania WGK |
1 |
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RTECS |
ES3450000 |
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F |
13 |
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Autoignition Temperature |
CDLXIV ° F |
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Capparis |
Ita |
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HazardClass |
3 |
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PackingGroup |
II |
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HS Code |
29121900 |
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Ancipitia substantiae Data |
590-86-3 (Malo Periculosam substantias Indicium) |
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Description |
Byoxidation paratus sit in isoamyl arcu. |
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Properties eget |
III, Methylbutyraldehydehas hauserant, potens, acribus, salsa malum, sicut divinum odorem spirare. Hoc compositis isalso nuntiavit habere fruity, pingue, animalis, amygdalus, impinguabitur locusta odoris suavissimi componendum. |
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Properties eget |
liquidwith fortis colore (aliquamdiu |
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Properties eget |
Is Isovaleraldehyde colore, odore similem humili solubility fluidi ofapples acrem. |
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usibus |
Isovaleraldehyde ismanufactured per ipsum et oxidizing isoamyl perchromate andsulfuric sodium acid. Isovaleraldehyde in praesenti est essentialis olea et aurantiacis, peppermint, lemon et aliis plantis et fructus. Eius principalis usus ut ELOGIUM anartificial flavor et in odoribus aevum. |
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usibus |
Artificialflavors et in odoribus aevum. |
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definitio |
ChEBI: hoc est Amethylbutanal Butanal substituimus per loco ad coetus yl 3. Itoccurs ut volatile constituent in oliveta flamma consumeret. |
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Praeparatio |
Per oxidatio ofisoamyl arcu. |
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Communia |
Lexus liquidwith infirma et suffocans odoris suavissimi componendum. Quod omni superenatat liquori. Asperioribus verbis ipsius fit et vapor. |
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Agrippina Minor aqua Aeris & |
Altus flammabilia. |
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Reactividad Profile |
Aldehyde Isovaleraldehyde ambiendis aruis. Aldehydes frequenter in se densum-orpolymerization profectae. Hae rationes profectae sunt exothermic; oftencatalyzed sunt ex aceto. Ut facile oxidized aldehydes carboxylic acids.Flammable / vel noxia vapores generantur compositum aldehydeswith Azo Diazo composita dithiocarbamates, nitrides et fortis reducingagents. Aldehydes caeli possunt dare vim suam, cum primum peroxo acida, andultimately carboxylate acida. Hae rationes profectae sunt activated Autooxidación bylight, catalyzed ex hiis quevis dubietas sales metallorum et non autocatalytic (catalyzed a products de reactionem). Quod etiam ex stabilimenta (facilisis) ut portarentur de aldehydes Autooxidación obstet. |
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salutem DISCRIMEN |
Inspiratione causeschest molestiae, nausea, vomitus, et in capitis dolore. Picis liquidae cutis contactus cum eyesor rodit. Pisces et os rodit et stomachum. |
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Praeparatio Products |
Acidum Isovaleric -> III-III-Methylbutyl methylbutanoate ->-VI-3H, isopropyl THIENO [2,3 D-] PYRIMIDIN-unum-IV -> amino-II-V-3-thiophene, isopropyl CARBOXYLICACID ETHYL ESTER -> octamylamine -> METHYL-IV-I-II-phenyl, PENTANOL -> hepten-II-III-VI-unus-Methyl -> V-Methyl-II-II, isopropyl hexenal, |
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et rudis materiae |
Methyl-I-III-butanol |
