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M32658

Sigma-Aldrich

3-Methyl-1-butanol

reagent grade, 98%

Sinonimo/i:

Isoamyl alcohol, Isopentyl alcohol

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About This Item

Formula condensata:
(CH3)2CHCH2CH2OH
Numero CAS:
123-51-3
Peso molecolare:
88.15
Beilstein:
1718835
Numero CE:
204-633-5
Numero MDL:
MFCD00002934
Codice UNSPSC:
12352001
ID PubChem:
329817968
NACRES:
NA.21
Prezzi e disponibilità al momento non sono disponibili

Grado

reagent grade

Livello qualitativo

100

Densità del vapore

3 (vs air)

Tensione di vapore

2 mmHg ( 20 °C)

Saggio

98%

Stato

liquid

Temp. autoaccensione

644 °F

Limite di esplosione

1.2-9 %, 100 °F

dilution

(for analytical testing)

Indice di rifrazione

n20/D 1.406 (lit.)

pH

5.6 (20 °C, 25 g/L)

P. ebollizione

130 °C (lit.)

Punto di fusione

−117 °C (lit.)

Densità

0.809 g/mL at 25 °C (lit.)

Stringa SMILE

CC(C)CCO

InChI

1S/C5H12O/c1-5(2)3-4-6/h5-6H,3-4H2,1-2H3
PHTQWCKDNZKARW-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

3-Methyl-1-butanol has been used in the preparation of bioactive beads (BABs) with uniform size for transformation.[1]

Azioni biochim/fisiol

3-Methyl-1-butanol is a pentanol isomer useful in biofuels.[2] It is used as a starting material for the production of isoamyl acetate, a flavoring agent applicable in the food industry.[3] 3-Methyl-1-butanol shows anti-fungal action by inhibiting the hyphal formation and reducing biofilm formation in Candida albicans.[4] It is also used in DNA extraction protocols.[5]

Avvertenze

Danger

Indicazioni di pericolo

H226,H315,H318,H332,H335

Classi di pericolo

Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

110.3 °F - closed cup

Punto d’infiammabilità (°C)

43.5 °C - closed cup

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
SHBN4545
SHBM7152
SHBQ5866
SHBL1515
SHBN7041

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Isoamyl alcohol for analysis EMSURE® ACS,Reag. Ph Eur

Supelco

1.00979

Isoamyl alcohol

Isopentyl acetate anhydrous, ≥99%

Sigma-Aldrich

306967

Isopentyl acetate

Alcool benzilico ACS reagent, ≥99.0%

Sigma-Aldrich

402834

Alcool benzilico

2-Methyl-1-butanol ≥99%

Sigma-Aldrich

133051

2-Methyl-1-butanol

3-Methyl-2-buten-1-ol 99%

Sigma-Aldrich

162353

3-Methyl-2-buten-1-ol

Vicente Pérez-Brocal et al.
Scientific reports, 10(1), 17377-17377 (2020-10-17)
Human lungs harbor a scarce microbial community, requiring to develop methods to enhance the recovery of nucleic acids from bacteria and fungi, leading to a more efficient analysis of the lung tissue microbiota. Here we describe five extraction protocols including
Metabolic engineering of Pichia pastoris for production of isopentanol (3-Methyl-1-butanol).
Siripong, et al.
Enzyme and Microbial Technology, 138, 109557-109557 (2021)
Michael Vogt et al.
Metabolic engineering, 38, 436-445 (2016-10-18)
The pentanol isomers 2-methyl-1-butanol and 3-methyl-1-butanol represent commercially interesting alcohols due to their potential application as biofuels. For a sustainable microbial production of these compounds, Corynebacterium glutamicum was engineered for producing 2-methyl-1-butanol and 3-methyl-1-butanol via the Ehrlich pathway from 2-keto-3-methylvalerate
Naoki Wada et al.
Methods in molecular biology (Clifton, N.J.), 847, 91-106 (2012-02-22)
The efficient transformation of plants with large DNA molecules containing a set of useful genes would provide vast possibilities for the genetic improvement of agricultural as well as nonagricultural plants. The development of the bioactive beads (BABs) transformation method has
Angélica de L Rodríguez López et al.
Antimicrobial agents and chemotherapy, 63(9) (2019-06-19)
Candida albicans is an opportunistic fungal pathogen responsible for mucosal candidiasis and systemic candidemia in humans. Often, these infections are associated with the formation of drug-resistant biofilms on the surfaces of tissues or medical devices. Increased incidence of C. albicans
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