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Documenti fondamentali

W222011

Sigma-Aldrich

Isobutirraldeide

greener alternative

natural, 96%, FG

Sinonimo/i:

2-metilpropanale, 2-metilpropionaldeide

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W222011-SAMPLE-K
CHF 62.60
100 G
CHF 169.00
1 KG
CHF 1’100.00

CHF 62.60


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Cambia visualizzazione
W222011-SAMPLE-K
CHF 62.60
100 G
CHF 169.00
1 KG
CHF 1’100.00

About This Item

Formula condensata:
(CH3)2CHCHO
Numero CAS:
Peso molecolare:
72.11
Numero FEMA:
2220
Beilstein:
605330
Numero CE:
N° CoE:
92c
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
5.004
NACRES:
NA.21

CHF 62.60


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Grado

FG
Fragrance grade
Halal
Kosher
natural

Livello qualitativo

agenzia

follows IFRA guidelines

Conformità normativa

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

Densità del vapore

2.5 (vs air)

Tensione di vapore

66 mmHg ( 4.4 °C)

Saggio

96%

Temp. autoaccensione

384 °F

Limite di esplosione

10 %, 25 °F
2 %, 32 °F

Caratteristiche più verdi

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

Indice di rifrazione

n20/D 1.374 (lit.)

P. ebollizione

63 °C (lit.)

Punto di fusione

−65 °C (lit.)

Solubilità

60 g/L at 25 °C

Densità

0.79 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

no known allergens

Categoria alternativa più verde

Organolettico

cocoa; pungent; brown

Stringa SMILE

[H]C(=O)C(C)C

InChI

1S/C4H8O/c1-4(2)3-5/h3-4H,1-2H3
AMIMRNSIRUDHCM-UHFFFAOYSA-N

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Descrizione generale

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

Applicazioni


  • Efficient total synthesis of pulchellalactam, a CD45 protein tyrosine phosphatase inhibitor.: Discusses a synthetic route involving isobutyraldehyde for developing inhibitors that have potential applications in biochemistry and medical research (Li WR et al., 2002).

Pittogrammi

FlameExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

-11.2 °F - closed cup

Punto d’infiammabilità (°C)

-24 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves


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Certificati d'analisi (COA)

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Addition of isobutyraldehyde to 1,2-bis(2-hydroxyphenyl)-1,2-diaminoethane (mother diamine) cleanly gives a stable, fused imidazolidine-dihydro-1,3-oxazine ring complex. However, vigorous heating of the fused ring complex gives the diaza-Cope rearrangement product with excellent yield and stereoselectivity. A variety of alkyl aldehydes have been
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Global climate change has stimulated efforts to reduce CO(2) emissions. One approach to addressing this problem is to recycle CO(2) directly into fuels or chemicals using photosynthesis. Here we genetically engineered Synechococcus elongatus PCC7942 to produce isobutyraldehyde and isobutanol directly
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Journal of the American Chemical Society, 125(9), 2475-2479 (2003-02-27)
Quantum mechanical calculations were employed to predict the ratio of four stereoisomeric products expected from two complex reactions involving the aldol reactions of cyclohexanone with benzaldehyde or with isobutyraldehyde catalyzed by (S)-proline. Experimental tests of these predictions provide an assessment
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