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Key Documents

Autres documents

901351

Sigma-Aldrich

Butan-1-ol

greener alternative

BioRenewable, ACS reagent, ≥99.4%

Synonyme(s) :

n-butanol, Alcool butylique

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About This Item

Formule linéaire :
CH3(CH2)3OH
Numéro CAS:
71-36-3
Poids moléculaire :
74.12
Numéro Beilstein :
969148
Numéro MDL:
MFCD00002964
Code UNSPSC :
12352001
Nomenclature NACRES :
NA.05

Qualité

ACS reagent

Niveau de qualité

200

Densité de vapeur

2.55 (vs air)

Pureté

≥99.4%

Forme

liquid

Température d'inflammation spontanée

649 °F

Limite d'explosivité

11.2 %

Caractéristiques du produit alternatif plus écologique

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

sustainability

Greener Alternative Product

renewable carbon content

100%

Impuretés

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

Résidus d'évap.

≤0.005%

Couleur

APHA: ≤10

Indice de réfraction

n20/D 1.399 (lit.)

Point d'ébullition

116-118 °C (lit.)

Pf

−90 °C (lit.)

Densité

0.81 g/mL at 25 °C (lit.)

Autre catégorie plus écologique

, Aligned

Chaîne SMILES 

CCCCO

InChI

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

Clé InChI

LRHPLDYGYMQRHN-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

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

Caractéristiques et avantages

  • 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

Autres remarques

To see other BioRenewable or Greener Solvents

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

FlameCorrosionExclamation mark
GHS02,GHS05,GHS07

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Central nervous system, Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

95.0 °F - Pensky-Martens closed cup

Point d'éclair (°C)

35 °C - Pensky-Martens closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
SHBK4584

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
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)
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
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