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Merck
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安全信息

901351

Sigma-Aldrich

正丁醇

greener alternative

BioRenewable, ACS reagent, ≥99.4%

别名:

丁醇, 正丁醇

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About This Item

线性分子式:
CH3(CH2)3OH
CAS号:
71-36-3
分子量:
74.12
Beilstein:
969148
MDL编号:
MFCD00002964
UNSPSC代码:
12352001
NACRES:
NA.05

等级

ACS reagent

质量水平

200

蒸汽密度

2.55 (vs air)

检测方案

≥99.4%

形式

liquid

自燃温度

649 °F

expl. lim.

11.2 %

环保替代产品特性

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

sustainability

Greener Alternative Product

renewable carbon content

100%

杂质

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

蒸发残留物

≤0.005%

颜色

APHA: ≤10

折射率

n20/D 1.399 (lit.)

bp

116-118 °C (lit.)

mp

−90 °C (lit.)

密度

0.81 g/mL at 25 °C (lit.)

环保替代产品分类

, Aligned

SMILES字符串

CCCCO

InChI

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

InChI key

LRHPLDYGYMQRHN-UHFFFAOYSA-N

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一般描述

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.

应用

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

特点和优势

  • 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

其他说明

To see other BioRenewable or Greener Solvents

相关产品

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说明
价格

警示用语：

Danger

危险分类

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

靶器官

Central nervous system, Respiratory system

WGK

WGK 1

闪点(°F)

95.0 °F

闪点(°C)

35 °C

法规信息

新产品

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分析证书(COA)

Lot/Batch Number

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  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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