Skip to Content
Merck
All Photos(1)

Documents

33065

Sigma-Aldrich

1-Butanol

puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥99.5% (GC)

Synonym(s):

n-Butanol, Butyl alcohol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)3OH
CAS Number:
Molecular Weight:
74.12
Beilstein:
969148
EC Number:
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent
puriss. p.a.

Agency

USP/NF
reag. ISO
reag. Ph. Eur.

vapor density

2.55 (vs air)

vapor pressure

5.5 mmHg

Assay

≥99.5% (GC)

form

liquid

autoignition temp.

649 °F

expl. lim.

11.2 %

impurities

≤0.001% non-volatile matter
≤0.005% free acid (as C3H7COOH)
≤0.01% n-butylaldehyde
≤0.03% aldehydes, ketones (as C3H7CHO)
≤0.05% 2-butanol
≤0.1% di-n-butylether
≤0.1% water (Karl Fischer)
≤0.15% iso-butanol

refractive index

n20/D 1.399 (lit.)

pH

7 (20 °C, 70 g/L)

bp

116-118 °C (lit.)

mp

−90 °C (lit.)

density

0.81 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg
B: ≤0.02 mg/kg
Ba: ≤0.1 mg/kg
Ca: ≤0.5 mg/kg
Cd: ≤0.05 mg/kg
Co: ≤0.02 mg/kg
Cr: ≤0.02 mg/kg
Cu: ≤0.02 mg/kg
Fe: ≤0.1 mg/kg
Mg: ≤0.1 mg/kg
Mn: ≤0.02 mg/kg
Ni: ≤0.02 mg/kg
Pb: ≤0.1 mg/kg
Sn: ≤0.1 mg/kg
Zn: ≤0.1 mg/kg

SMILES string

CCCCO

InChI

1S/C4H10O/c1-2-3-4-5/h5H,2-4H2,1H3

InChI key

LRHPLDYGYMQRHN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

1-Butanol is a linear alcohol. Its biosynthesis from glucose using a bioengineered Escherichia coli strain has been reported. Its reaction with diisocyanates in the presence of triethylamine (catalyst) has been investigated by volumetric method. Its dehydration reaction has been employed as a standard reaction to evaluate the acidic and basic characteristics of various silica-aluminas.

Application

1-Butanol may be used for the solid acid (acidic salt of H3PW12O40, Cs2.5H0.5PW12O40) catalyzed esterification of acrylic acid.

Other Notes

The article number 33065-4X2.5L-R will be discontinued. Please order the single bottle 33065-2.5L-R which is physically identical with the same exact specifications.
The article number 33065-6X1L-R will be discontinued. Please order the single bottle 33065-1L-R which is physically identical with the same exact specifications.

greener alternative product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

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

Target Organs

Central nervous system, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

95.0 °F - Pensky-Martens closed cup

Flash Point(C)

35 °C - Pensky-Martens closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

The kinetics of the triethylamine-catalyzed reaction of diisocyanates with 1-butanol in toluene.
Burkus J and Eckert CF.
Journal of the American Chemical Society, 80(22), 5948-5950 (1958)
Acid-base properties of silica-aluminas: use of 1-butanol dehydration as a test reaction.
Berteau P, et al.
Applied Catalysis, 70(1), 307-323 (1991)
Liquid phase esterification of acrylic acid with 1-butanol catalyzed by solid acid catalysts.
Chen X, et al.
Applied Catalysis A: General, 180(!), 261-269 (1999)
Prasenjit Seal et al.
The journal of physical chemistry. A, 117(2), 275-282 (2012-12-19)
In the present work, we study the H atom abstraction reactions by hydroxyl radical at all five sites of 1-butanol. Multistructural variational transition state theory (MS-VTST) was employed to estimate the five thermal rate constants. MS-VTST utilizes a multifaceted dividing
C R Shen et al.
Metabolic engineering, 10(6), 312-320 (2008-09-09)
Production of higher alcohols via the keto-acid intermediates found in microorganism's native amino-acid pathways has recently shown promising results. In this work, an Escherichia coli strain that produces 1-butanol and 1-propanol from glucose was constructed. The strain first converts glucose

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service