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.
901351
1-Butanol
100% BioRenewable, reagent grade, ≥99.4%
Synonym(s):
n-Butanol, Butyl alcohol
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About This Item
Linear Formula:
CH3(CH2)3OH
CAS Number:
Molecular Weight:
74.12
NACRES:
NA.05
UNSPSC Code:
12352001
Beilstein/REAXYS Number:
969148
MDL number:
Assay:
≥99.4%
Grade:
reagent grade
Bp:
116-118 °C (lit.)
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grade
reagent grade
Quality Level
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%
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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.
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:
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
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Product No.
Description
Pricing
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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
Storage Class
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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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
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
Related Content
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 901351-4L | 04061837563287 |
| 901351-1L | 04061837563270 |
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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.
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What is a BioRenewable solvent?
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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.
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