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901351

Sigma-Aldrich

1-Butanol

greener alternative

BioRenewable, ACS reagent, ≥99.4%

Sinônimo(s):

n-Butanol, Álcool butílico

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About This Item

Fórmula linear:
CH3(CH2)3OH
Número CAS:
71-36-3
Peso molecular:
74.12
Beilstein:
969148
Número MDL:
MFCD00002964
Código UNSPSC:
12352001
NACRES:
NA.05

grau

ACS reagent

Nível de qualidade

200

densidade de vapor

2.55 (vs air)

Ensaio

≥99.4%

forma

liquid

temperatura de autoignição

649 °F

Lim. expl.

11.2 %

características do produto alternativo mais ecológico

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

sustainability

Greener Alternative Product

renewable carbon content

100%

Impurezas

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

resíduo de evaporação

≤0.005%

cor

APHA: ≤10

índice de refração

n20/D 1.399 (lit.)

pb

116-118 °C (lit.)

pf

−90 °C (lit.)

densidade

0.81 g/mL at 25 °C (lit.)

categoria alternativa mais ecológica

, Aligned

cadeia de caracteres SMILES

CCCCO

InChI

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

chave InChI

LRHPLDYGYMQRHN-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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

Características e benefícios

  • 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

Outras notas

To see other BioRenewable or Greener Solvents

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Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Central nervous system, Respiratory system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

95.0 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

35 °C - Pensky-Martens closed cup

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
SHBK4584

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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)
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
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