Passa al contenuto
Merck
Tutte le immagini(5)

Key Documents

901351

Sigma-Aldrich

1-butanolo

greener alternative

BioRenewable, ACS reagent, ≥99.4%

Sinonimo/i:

n-butanolo, Alcol butilico

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula condensata:
CH3(CH2)3OH
Numero CAS:
Peso molecolare:
74.12
Beilstein:
969148
Numero MDL:
Codice UNSPSC:
12352001
NACRES:
NA.05

Grado

ACS reagent

Livello qualitativo

Densità del vapore

2.55 (vs air)

Saggio

≥99.4%

Forma fisica

liquid

Temp. autoaccensione

649 °F

Limite di esplosione

11.2 %

Caratteristiche più verdi

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

sustainability

Greener Alternative Product

renewable carbon content

100%

Impurezze

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

Residuo dopo evaporazione

≤0.005%

Colore

APHA: ≤10

Indice di rifrazione

n20/D 1.399 (lit.)

P. eboll.

116-118 °C (lit.)

Punto di fusione

−90 °C (lit.)

Densità

0.81 g/mL at 25 °C (lit.)

Categoria alternativa più verde

Stringa SMILE

CCCCO

InChI

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

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

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.

Applicazioni

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

Caratteristiche e vantaggi

  • 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

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Central nervous system, Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

95.0 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

35 °C - Pensky-Martens closed cup


Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number

Non trovi la versione di tuo interesse?

Se hai bisogno di una versione specifica, puoi cercare il certificato tramite il numero di lotto.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 9

1 of 9

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

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.