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1-Butanol

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Company Name: Henan DaKen Chemical CO.,LTD.
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Products Intro: Product Name:1-Butanol
CAS:71-36-3
Purity:99% Package:100g,500g,1kg,5kg,10kg
Company Name: Shanghai Bojing Chemical Co.,Ltd.
Tel: +86-21-37122233
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Products Intro: Product Name:1-Butanol
CAS:71-36-3
Purity:99% Package:1kg;25kg;200kg Plastic drum Remarks:Colorless liquid
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: 0371-55170693
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Products Intro: CAS:71-36-3
Purity:99% Package:500G;1KG;5KG;25KG
Company Name: Mainchem Co., Ltd.
Tel: +86-0592-6210733
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Products Intro: Product Name:1-Butanol
CAS:71-36-3
Purity:99%
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
Tel: 86-0551-65418684 18949823763
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Products Intro: Product Name:n-butanol
CAS:71-36-3
Purity:99% Package:1KG;1USD

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1-Butanol Chemical Properties
Melting point -89 °C
Boiling point 117.6 °C
density 0.81 g/mL at 25 °C(lit.)
vapor density 2.55 (vs air)
refractive index n20/D 1.399(lit.)
FEMA 2178 | BUTYL ALCOHOL
Fp 95 °F
storage temp. Store at RT.
solubility water: soluble
form Liquid
color APHA: ≤10
Relative polarity0.586
PH7 (70g/l, H2O, 20℃)
explosive limit1.4-11.3%(V)
Water Solubility 80 g/L (20 ºC)
Sensitive Moisture Sensitive
Merck 14,1540
BRN 969148
Stability:Stable. Incompatible with strong acids, strong oxidizing agents, aluminium, acid chlorides, acid anhydrides, copper, copper alloys. Flammable.
CAS DataBase Reference71-36-3(CAS DataBase Reference)
NIST Chemistry Reference1-Butanol(71-36-3)
EPA Substance Registry System1-Butanol(71-36-3)
Safety Information
Hazard Codes Xn,T,F
Risk Statements 10-22-37/38-41-67-39/23/24/25-23/24/25-11
Safety Statements 13-26-37/39-46-7/9-45-36/37-16-7
RIDADR UN 1120 3/PG 3
WGK Germany 1
RTECS EO1400000
TSCA Yes
HazardClass 3
PackingGroup III
Hazardous Substances Data71-36-3(Hazardous Substances Data)
ToxicityLD50 orally in rats: 4.36 g/kg (Smyth)
MSDS Information
1-Butanol Usage And Synthesis
Characteristics and history of discovery1-Butanol is a type of alcohol with four carbon atoms being contained per molecule. Its molecular formula is CH3CH2CH2CH2OH with three isomers, namely iso-butanol, sec-butanol and tert-butanol. It is colorless liquid with alcohol odor.
It has the boiling point of being 117.7 ℃, the density (20 ℃) being ​​0.8109g/cm3, the freezing point being-89.0 ℃, flash point being 36~38 ℃, self-ignition point being 689F and the refractive index being (n20D) 1.3993. At 20 ℃, its solubility in water is 7.7% (by weight) while the water solubility in 1-butanol was 20.1% (by weight). It is miscible with ethanol, ether and other kinds of organic solvents. It can be used as the solvents of a variety of paints and the raw material for producing the plasticizers, dibutyl phthalate. It can also be used for the manufacture of butyl acrylate, butyl acetate, and ethylene glycol butyl ether and also used as the extract of intermediates of organic synthesis and biochemical drugs and can also used in the manufacture of surfactants. Its steam can form explosive mixtures with air with the explosion limit being 3.7%~10.2% (volume fraction).
1-butanol was first discovered by C-A. Wurtz (French) from the fusel oil obtained from the fermentation process of alcohol in 1852. In 1913, the British Strange-Graham Companies have used corn as raw material for production of acetone through the fermentation process with butanol being the main byproduct. Later, due to the increasing demand for butanol, the fermentation production factory began to mainly synthesize n-butanol with acetone and ethanol being the major byproduct. During the Second World War, the German chemical company (Ruhr) began to apply propylene carboxyl method for the production of 1-butanol. With the rise of the oil industry in 1950s, the 1-butanol synthesis method had gotten rapid development with the propylene carboxyl method having the fastest speed.
Preparation of water saturated 1-butanol solutionAdd 21 mL of water and 100 mL of 1-butanol to separating funnel of 150 mL, shake for 3 min, stand for layering; and then remove the lower layer with the upper layer being water-saturated 1-butanol solution. (The density of water: 1 g/ml; 1-butanol density: 0.808~0.811 g/ml).
Content AnalysisFor the determination of 1-butanol and volatile impurities according to the general gas chromatography (GT-10), use the following conditions:
Column steel column, length: 1.8m; inner diameter: 6.4mm, the packing material should be 10% polyethylene glycol 400M (PEG 400M) with the carrier being 60/80 mesh diatomaceous soil carrier.
Carrier gas: Helium with a flow rate of 45ml/min. Detector: Flame ionization type.
Injector temperature 150 ℃, column temperature 90 0 ℃ detector 150 ℃.
The above information is edited by the Chemicalbook of Dai Xiongfeng.
ToxicityADI value is not specified (FAO/WHO, 1994).
GRAS (FEMA).
LD50: 790 mg/kg (rat, oral).
UsesIt can be used as chromatography analysis reagents and also applied to organic synthesis, etc.
Butanol is the allowable food flavors documented in the "food additives health standards" of China. It is mainly used for the preparation of food flavors of bananas, butter, cheese and whiskey. For the candy, the usage amount should be 34mg/kg; for baked foods, it should be 32mg/kg; for soft drinks, it should be 12mg/kg; for cold drinks, it should be 7.0mg/kg; for the cream, it should be 4.0mg/kg; for alcohol, it should be 1.0mg/kg.
Butanol can be used as the intermediates of herbicide 2,4-D butyl ester, butachlor, fluazifop and fluazifop P butyl.
GB 2760-96 provides it be the food flavor allowed by using it. It can be mainly used for the preparation of bananas, butter, cheese, whiskey and other flavor. It can also be used as extraction-purpose solvent and pigment diluent.
It is mainly used for the manufacture of the n-butyl plasticizers of phthalic acid, aliphatic dicarboxylic acid and phosphoric acid that are widely applied to various kinds of plastic and rubber products. It can also be used as the raw material of producing butyraldehyde, butyric acid, butyl-amine and butyl lactate in the field of organic synthesis. It can also be used as the extraction agent of oil, drugs (such as antibiotics, hormones and vitamins) and spices as well as the alkyd paint additives. It can be used as the solvent of organic dyes and printing ink and de-waxing agent.
It can be used for the production of the plasticizers of butyl acetate, dibutyl phthalate and phosphate and can also be used in the production of melamine resin, crylic acid, and epoxy varnish, etc.
Production methodThere are several methods for their preparation.
Fermentation
In the past, the production of butanol has also used potatoes, grain or sugar as raw material and through their hydrolysis fermentation. The resulting product from the fermentation broth contains a butanol content of 54.8%~58.5%, acetone content of 30.9%~33.7%, and the ethanol content of 7.8%-14.2%. With the development of petrochemical industry, fermentation method has been gradually phased out. The reaction equation is as follows: (C6H10O5) n [n (H2O)] → [strain] n-C6H12O6 [fermentation] → CH3COCH3 + C4H9OH + C2H5OH
The resulted fermentation broth was further fractionated to obtain acetone, ethanol and n-butanol separately.
Acetaldehyde method
Take acetaldehyde as raw material, add dilute alkali solution to give 2-hydroxybutyraldehyde at temperature below 20 ℃ with the reaction being stopped upon reaching 50%. Use alkali to neutralize the acid and recycle the unreacted acetaldehyde and extract the 2-hydroxybutyraldehyde. Then use acidic catalyst such as sulfuric acid and acetic acid for dehydration to obtain crotonaldehyde at 105~137 ℃, then use copper complex catalyst for hydrogenation at 160~240 ℃ to obtain the crude butyraldehyde and 1-butanol with distillation to obtain the products. CH3CH = CHCHO + H2 [catalyst] CH3CH2CH2CHO + CH3CH2CH2CH2OH
Its synthesis method including the following several ways:
Fermentation and Propylene carbonyl synthesis
Put propylene, carbon monoxide and hydrogen to the catalytic bed for reaction with catalyst being zeolite for absorbing cobalt salt or fatty acid cobalt with the reaction temperature being 130~160 ℃ and the reaction pressure being 20~25MPa. The reaction can generate n-butyraldehyde and iso-butyraldehyde with separation via distillation and further catalytic hydrogenation of the n-butyraldehyde to obtain the 1-butanol. CH3CH2CH2CHO + H2 → CH3CH2CH2CH2OH
You can alternatively use low pressure method with first-step method of propylene, carbon monoxide and water for synthesizing the butanol with the reaction temperature being 100~104 ℃ and pressure being 1.5MPa. It applies the mixture of iron pentacarbonyl, n-butyl pyrrolidine and water. However, the one-way conversion of the propylene is low with only 8% to 10%. Reaction equation: CH3CH = CH2 + 3CO + 2H2O → n-C4H9OH + 2CO2
Descriptionn-Butyl alcohol is a colourless flammable liquid with strong alcoholic odour. n-Butyl alcohol is a highly refractive liquid and burns with a strongly luminous flame. It is incompatible with strong acids, strong oxidising agents, aluminium, acid chlorides, acid anhydrides, copper, and copper alloys. n-Butyl alcohol has an extensive use in a large number of industries. For instance, it is used as solvent in industries associated with the manufacturing of paints, varnishes, synthetic resins, gums, pharmaceuticals, vegetable oils, dyes, and alkaloids. n-Butyl alcohol finds its use in the manufacture of artificial leather, rubber, plastic cements, shellac, raincoats, perfumes, and photographic films.
Chemical PropertiesColorless liquid
UsesSuitable for HPLC, spectrophotometry, environmental testing
DefinitionChEBI: A primary alcohol that is butane in which a hydrogen of one of the methyl groups is substituted by a hydroxy group. It it produced in small amounts in humans by the gut microbes.
UsesAs solvent for fats, waxes, resins, shellac, varnish, gums etc.; manufacture of lacquers, rayon, detergents, other butyl Compounds; in microscopy for preparing paraffin imbedding materials.
General DescriptionColorless liquid. Used in organic chemical synthesis, plasticizers, detergents, etc.
Air & Water ReactionsHighly flammable. Soluble in water.
Reactivity Profile1-Butanol attacks plastics. [Handling Chemicals Safely 1980. p. 236]. Mixtures with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. May form explosive butyl hypochlorite by reacting with hypochlorous acid. May form butyl explosive butyl hypochlorite with chlorine.
Health HazardAnesthesia, nausea, headache, dizziness, irritation of respiratory passages. Mildly irritating to the skin and eyes.
Fire HazardHIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
Purification MethodsDry it with MgSO4, CaO, K2CO3, or solid NaOH, followed by refluxing with, and distillation from, small amounts of calcium, magnesium activated with iodine, or aluminium amalgam. It can also be dried with molecular sieves, or by refluxing with n-butyl phthalate or succinate. (For method, see Ethanol.) n-Butanol can also be dried by efficient fractional distillation, water passing over in the first fraction as a binary azeotrope (contains about 37% water). An ultraviolet-transparent distillate has been obtained by drying with magnesium and distilling from sulfanilic acid. To remove bases, aldehydes and ketones, the alcohol is washed with dilute H2SO4, then NaHSO4 solution; esters are removed by boiling for 1.5hours with 10% NaOH. It has also been purified by adding 2g NaBH4 to 1.5L butanol, gently bubbling with argon and refluxing for 1 day at 50o. Then adding 2g of freshly cut sodium (washed with butanol) and refluxed for 1day. Distil and collect the middle fraction [Jou & Freeman J Phys Chem 81 909 1977]. [Beilstein 1 IV 1506.]
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