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Merck

901351

Butan-1-ol

greener alternative

BioRenewable, 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:
Poids moléculaire :
74.12
NACRES:
NA.05
UNSPSC Code:
12352001
Beilstein/REAXYS Number:
969148
MDL number:
Assay:
≥99.4%
Grade:
ACS reagent
Bp:
116-118 °C (lit.)
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Nom du produit

Butan-1-ol, BioRenewable, ACS reagent, ≥99.4%

SMILES string

CCCCO

InChI

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

InChI key

LRHPLDYGYMQRHN-UHFFFAOYSA-N

grade

ACS reagent

vapor density

2.55 (vs air)

assay

≥99.4%

form

liquid

autoignition temp.

649 °F

expl. lim.

11.2 %

greener alternative product characteristics

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

renewable carbon content

100%

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.)

bp

116-118 °C (lit.)

mp

−90 °C (lit.)

density

0.81 g/mL at 25 °C (lit.)

greener alternative category

Quality Level

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Application

Drop-in replacement for all 1-Butanol applications. Does not affect change in procedure or equipment.

1-Butanol may be used in applications such as:
  • Extraction and purification of compounds
  • Solvent in chemical synthesis
  • Intermediate in polymer synthesis
  • Adhesives and sealants formulation
  • Coatings

Features and Benefits

  • ASTM D6866 - Standard Test Methods for Determining the Biobased Content
  • Renewable Carbon Content – ≥99.9%
  • Made from Renewable Resource
  • Replacement for Petroleum-based 1-Butanol

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is 100% biorenewable and thus aligns with "Safer Solvents and Auxiliaries" and "Use of Renewable Feedstocks". Click here for more information.
This ACS grade 1-Butanol is a drop-in replacement for traditional 1-Butanol applications. Made from 100% renewable carbon (verified through C14 ASTM D6866-16 testing) and produced in an environmentally-friendly way which reduces the carbon footprint of production and reduces reliance on fossil-fuels.
It is also free from many contaminants that are present in petroleum derived 1-Butanol, such as isobutanol and aldehydes.

signalword

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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Consulter la Bibliothèque de documents

  1. What is a BioRenewable solvent?

    BioRenewable solvents are sourced from renewable and sustainable biobased materials, such as soy/palm oil, wood waste, hay or corn byproducts, etc. It is important to highlight that our BioRenewable products do not compete with food production.

  2. Why should you use BioRenewable solvents?

    You will contribute to create a sustainable world, significantly lowering environmental impact. Biorenewable solvents also decrease petroleum sources dependency, have higher recovery rates, and/or are safer for handling and disposal.

  3. Do BioRenewable solvents have a similar quality to petroleum-based solvents?

    BioRenewable solvents can have the same or higher purity level compared to traditional solvents. These solvents are free of the many byproducts of petroleum manufacturing, such as benzene, aldehydes, and ethers.

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
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)
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
Joel G Davis et al.
Nature, 491(7425), 582-585 (2012-11-23)
Hydrophobic hydration is considered to have a key role in biological processes ranging from membrane formation to protein folding and ligand binding. Historically, hydrophobic hydration shells were thought to resemble solid clathrate hydrates, with solutes surrounded by polyhedral cages composed

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