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Merck

320021

Sigma-Aldrich

3-Methyl-1-butanol

ACS reagent, ≥98.5%

동의어(들):

Isoamyl alcohol, Isopentyl alcohol

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
(CH3)2CHCH2CH2OH
CAS 번호:
Molecular Weight:
88.15
Beilstein:
1718835
EC Number:
MDL number:
UNSPSC 코드:
12352001
PubChem Substance ID:
NACRES:
NA.21
Grade:
ACS reagent
Bp:
130 °C (lit.)
Vapor pressure:
2 mmHg ( 20 °C)
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도움 문의

Grade

ACS reagent

Quality Level

vapor density

3 (vs air)

vapor pressure

2 mmHg ( 20 °C)

분석

≥98.5%

양식

liquid

autoignition temp.

644 °F

expl. lim.

1.2-9 %, 100 °F

dilution

(for analytical testing)

불순물

≤0.002 meq/g Titr. acid
≤0.1% carbonyl (as HCHO)
≤0.2% acids and esters (as amyl acetate)
≤0.5% water

증발 잔류물

≤0.003%

refractive index

n20/D 1.406 (lit.)

pH

5.6 (20 °C, 25 g/L)

bp

130 °C (lit.)

mp

−117 °C (lit.)

density

0.809 g/mL at 25 °C (lit.)

SMILES string

CC(C)CCO

InChI

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

InChI key

PHTQWCKDNZKARW-UHFFFAOYSA-N

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일반 설명

3-methyl-1-butanol is a clear, colorless alcohol. It is one of several isomers of amyl alcohol. It is commonly used as a solvent in various applications, such as inks, coatings, and pharmaceutical preparations.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

애플리케이션

3-Methyl-1-butanol is used as a:
  • Dissolution of a wide range of organic compounds and is often employed for extraction, dilution, and preparation of samples for analysis.
  • Starting material or reagent in organic synthesis. It can be incorporated into various reactions to introduce the isoamyl group or alcohol functionality into target molecules.

픽토그램

FlameCorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

110.3 °F - closed cup

Flash Point (°C)

43.5 °C - closed cup


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문서 라이브러리 방문

Mary J Dunlop et al.
Molecular systems biology, 7, 487-487 (2011-05-11)
Many compounds being considered as candidates for advanced biofuels are toxic to microorganisms. This introduces an undesirable trade-off when engineering metabolic pathways for biofuel production because the engineered microbes must balance production against survival. Cellular export systems, such as efflux
Kazushi Yoshida et al.
Nature communications, 3, 739-739 (2012-03-15)
The same odorant can induce attractive or repulsive responses depending on its concentration in various animals including humans. However, little is understood about the neuronal basis of this behavioural phenomenon. Here we show that Caenorhabditis elegans avoids high concentrations of
Frédéric Ravyts et al.
Food microbiology, 27(7), 945-954 (2010-08-07)
Differences in the production of bacterial metabolites with potential impact on fermented sausage flavour were found in meat simulation medium when comparing different strains of Staphylococcus xylosus and Staphylococcus carnosus as starter cultures. Overall, higher levels of 3-methyl-1-butanol and acetoin
Niels O Verhulst et al.
Malaria journal, 10, 28-28 (2011-02-10)
Anopheles gambiae sensu stricto is considered to be highly anthropophilic and volatiles of human origin provide essential cues during its host-seeking behaviour. A synthetic blend of three human-derived volatiles, ammonia, lactic acid and tetradecanoic acid, attracts A. gambiae. In addition
Silvio Zaina et al.
Circulation. Cardiovascular genetics, 7(5), 692-700 (2014-08-06)
Epigenetic alterations may contribute to the development of atherosclerosis. In particular, DNA methylation, a reversible and highly regulated DNA modification, could influence disease onset and progression because it functions as an effector for environmental influences, including diet and lifestyle, both

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