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360465

Butan-1-ol

ACS reagent, ≥99.4%

Synonyme(s) :

n-butanol, Alcool butylique

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A propos de cet article

Formule linéaire :
CH3(CH2)3OH
Numéro CAS:
71-36-3
Poids moléculaire :
74.12
UNSPSC Code:
12352001
NACRES:
NA.21
PubChem Substance ID:
329755258
EC Number:
200-751-6
Beilstein/REAXYS Number:
969148
MDL number:
MFCD00002964
Assay:
≥99.4%
Grade:
ACS reagent
Bp:
116-118 °C (lit.)
Vapor pressure:
5.5 mmHg
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grade

ACS reagent

Quality Level

200

vapor density

2.55 (vs air)

vapor pressure

5.5 mmHg

assay

≥99.4%

form

liquid

autoignition temp.

649 °F

expl. lim.

11.2 %

dilution

(for analytical testing)

impurities

≤0.0008 meq/g Titr. acid, ≤0.01% butyraldehyde, ≤0.1% water, ≤0.2% butyl ether

evapn. residue

≤0.005%

color

APHA: ≤10

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.)

SMILES string

CCCCO

InChI

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

InChI key

LRHPLDYGYMQRHN-UHFFFAOYSA-N

General description

1-Butanol is the primary alcohol that can be used as a carrier liquid for the extraction of synthetic resins, natural resins, paints, essential oils, gums, coatings, dyes, camphor, and alkaloids. It can be used as an extracting solvent for hormones, vitamins, and antibiotics. In the production of paint removers and industrial cleaners 1-butanol is being used. It is also used in the manufacture of rubber products, plastics, coating solvents, and dibutyl phthalate.
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.

Application

1-Butanol can be used:
  • As a solvent along with the water in the delignification of sugar cane bagasse.
  • As a both reagent and reaction medium in the synthesis of zinc oxide nanoparticles from zinc acetylacetonate hydrate as precursor.
  • As an additive in the diesel-biodiesel-butanol tertiary blend which leads to fuel sustainability.
  • As a reactant in the enzyme catalyzed esterification reaction of oleic acid to butyl oleate.

Other Notes

Go to our BioRenewable Alternative 1-Butanol - 901351

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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

Classe de stockage

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

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Contenu apparenté

M-Bottle for Safe Handling of Solvents

The 4L M-Bottle provides safe handling of solvents due to an innovative solvent bottle design with sealing technology to eliminate leaks and reduce risks in solvent dispensing.

E Gavini et al.
International journal of pharmaceutics, 307(1), 9-15 (2005-11-01)
The nasal route is used both for local therapies and, more recently, for the systemic administration of drugs, as well as for the delivery of peptides and vaccines. In this study the nasal administration of Carbamazepine (CBZ) has been studied
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)
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
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Numéro d'article de commerce international

RéférenceGTIN
360465-18L-CS04061837911019
360465-2.5L04061831817850
360465-4X2.5L04061831817904
360465-1L04061831817836
360465-4X4L04061831817966
360465-500ML04061831817973