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Levulinic acid

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CAS:123-76-2
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CAS:123-76-2
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Products Intro: Product Name:Levulinic acid
CAS:123-76-2
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Levulinic acid manufacturers

  • Levulinic acid
  • $20.00 / Kg/Drum
  • 2021-12-03
  • CAS:123-76-2
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  • 2021-11-08
  • CAS:123-76-2
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  • Levulinic acid
  • $555.00 / Kg/Bag
  • 2021-11-02
  • CAS:123-76-2
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Related articles

Levulinic acid Basic information
Chemical Properties Uses Application Preparation Content analysis Toxicity Usage limit
Product Name:Levulinic acid
Synonyms:2-Acetopropionicacid;aevuL;Levulinic acid 4-oxopentanoic acid;sodium 4-oxopentanoate;4-Keto-n-valericacid;4-Oxo-pentanoic acid (levulinic acid);4-oxo-pentanoicaci;4-oxovaleric
CAS:123-76-2
MF:C5H8O3
MW:116.12
EINECS:204-649-2
Product Categories:ACETYLGROUP;Intermediates;Building Blocks;C1 to C5;Carbonyl Compounds;Pharma material;Fatty & Aliphatic Acids, Esters, Alcohols & Derivatives;Biochemistry;Reagents for Oligosaccharide Synthesis;Dextrins、Sugar & Carbohydrates;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
Mol File:123-76-2.mol
Levulinic acid Structure
Levulinic acid Chemical Properties
Melting point 30-33 °C (lit.)
Boiling point 245-246 °C (lit.)
density 1.134 g/mL at 25 °C (lit.)
vapor pressure 1 mm Hg ( 102 °C)
refractive index n20/D 1.439(lit.)
FEMA 2627 | LEVULINIC ACID
Fp 280 °F
storage temp. Store below +30°C.
solubility 675g/l
form Liquid After Melting
pkapKa 4.65(H2O,t = 25,c=0.03-0.001) (Uncertain)
color Clear yellow
Water Solubility Soluble in water ( 675g/L at 20°C).
Sensitive Light Sensitive
Merck 14,5472
JECFA Number606
BRN 506796
InChIKeyJOOXCMJARBKPKM-UHFFFAOYSA-N
CAS DataBase Reference123-76-2(CAS DataBase Reference)
NIST Chemistry ReferencePentanoic acid, 4-oxo-(123-76-2)
EPA Substance Registry SystemLevulinic acid (123-76-2)
Safety Information
Hazard Codes Xn,C
Risk Statements 22-36/37/38-34-R34-R22
Safety Statements 26-45-36/37/39-S45-S36/37/39-S26
RIDADR 3261
WGK Germany 3
RTECS OI1575000
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29183000
ToxicityLD50 orally in Rabbit: 1850 mg/kg LD50 dermal Rabbit > 5000 mg/kg
MSDS Information
ProviderLanguage
Levulic acid English
SigmaAldrich English
ACROS English
ALFA English
Levulinic acid Usage And Synthesis
Chemical PropertiesWhite flake crystals, hygroscopic. clear yellowish liquid after melting.It is easily soluble in water and alcohol, ether organic solvents.
Levulinic acid
Levulinic acid conventionally is derived from refined petroleum but technological advances now permit the production of levulinic acid from biomass. Suitable feedstocks from the forest industry include pulp and paper mill residues, sawmill and logging residues, and solid municipal waste. It takes approximately 2 kg of cellulose to produce 1 kg of levulinic acid (US Department of Energy 1998). Obtaining enough raw materials to support the production of levulinic acid from biomass is not a foreseeable concern; Canada currently produces over 75 million tonnes of logging residues annually which, in turn, could produce 19 million tonnes of levulinic acid.
UsesLevulinic acid is a biomass product and its derivatives, such as ethyl levulinate and alkyl levulinate, can be used as fuel additives.
levulinic acid is used for calcium levulinate in pharmaceuticals, as esters in solvents and plasticizers, and for making valerolactone. As its uses expand, it will probably be made from cellulosic wastes. Mesitonic acid, a homolog of levulinic acid is obtained by boiing mesityl oxide with KCN.
Hydrogenation of levulinic acid can produce other useful chemicals. Valeric-g-lactone, which is an effective solvent with extensive uses, can be obtained in very high yields. This compound may be hydrogenated to 1,4-pentandiol, which upon dehydration yields 1,3-pentadine (piperylene). Piperylene is known to polymerize to a rubbery mass and is therefore a source of synthetic rubber (Ghorpade and Hanna 1997).
Levulinic acid is a precursor for the synthesis of useful intermediates such as γ-valerolactone, ethyl levulinate, pentanoic acid and 2-methyl-tetrahydrofuran. Derivatization and esterification of levulinic acid results in potential biofuels.
It can also be used in:
The preparation of catalytic composite to synthesize 5-hydroxymethylfurfural and furfural.
The synthesis of a commercial fragrance, fraistone.
The synthesis of pyrrolidone derivatives via reductive amination.
The total synthesis of mycobacterial arabinogalactan.
ApplicationIt can be used as the raw materials of medicine, spices and paint, and used as solvent.
This product has wide applications. Levulinic acid can be used as both a carboxylic acid and can also be used as a ketone for reaction for making various kinds of products through esterification, halogenation, hydrogenation, oxidation dehydrogenation, condensation, etc., including resins, pharmaceuticals, spices, solvents, rubber and plastic additives, lubricants additives, surfactants and so on. In the pharmaceutical industry, its calcium salt (calcium fructose) can be used for intravenous injection. As a nutritional medicine, it helps to boost the formation of bone and maintain the normal excitability of nerves and muscles. It can also used for the production of indomethacin and plant hormones. Levulinic acid manufactured bisphenol acid can be made of water-soluble resin, used in the paper industry to produce filter paper. Levulinic acid is also an intermediate of pesticides and dyes.
Used for biochemical reagents, but also for organic synthesis
It can be used as an important chemical raw material or solvents. It can be used for the manufacturing of medicine (intravenous injection, indomethacin, etc.), resin (bisphenol acid water-soluble resin), spices (spices or tobacco spices), paint, paint, pesticides, and surfactants.
It can be used for biochemical research; manufacturing of esters and drugs. It is also the inhibitor of chlorophyll synthesis.
PreparationThe residue during the manufacturing of furfural with cotton seed shell or corncob sugar (furfural residue) or waste taro residue, through pressured hydrolysis with dilute acid, can be used to produce levulinic acid. The furfural residue was added to 10% dilute hydrochloric acid, the solidified solution was 1: 1.75, mixed and put into the hydrolysis pot, steamed at a pressure of 0.2MPa for 8-10 h. The diluted solution is then filtered and concentrated to a concentration of about 50%. It is further subject to vacuum distillation for collecting the fraction above 130 ℃ (2.67kPa) to obtain the finished product. Raw material consumption quota: potato tacar 7,000 kg/t, hydrochloric acid (fold 100%) 1800kg/t. Another method is manufacturing through the rearrangement and hydrolysis of sugar alcohol.
4% hydrochloric acid solution was added to the reaction pot, stir and heat to 97-100 ℃, slowly add the mixture of furfuryl alcohol, ethanol and water. After addition, stir 30 min. The filtrate was concentrated at 80 ° C (21.3 kPa) under reduced pressure to give crude levulinic acid. Then apply vacuum distillation, collect the fraction of 160-170 ° C (2.67kPa), and then re-distill once, to obtain the refined levulinic acid with the yield of about 75%.
Content analysisAccurately weigh about 1.0 g of the sample, and put it into a 250ml Erlenmeyer flask containing 75~100ml water, add phenolphthalein test solution; apply 0.5 mol/L sodium hydroxide for titration to until it began to appear pink and maintain 15 s. Each mL of 0.5mol/L sodium hydroxide solution is equivalent to 58.08mg of the goods.
ToxicityGRAS (FEMA).
Usage limitFEMA (mg/kg): Beverage, cold drink, 14.0; Candy, baked goods, 53.0; Gelatin, pudding, 4.0.
FDA, §172.515 (2000): take proper amount as limit.
DescriptionLevulinic acid has a tart, whiskey taste. It may be synthesized by the action of more or less concentrated HCL on sucrose, glucose, or fructose; hence, its reported presence in caramels.
Chemical PropertiesLevulinic acid has a tart, whiskey taste.
OccurrenceReported found in papaya, wheat bread, rice, sake and Chinese quince.
UsesReplenisher (calcium).
PreparationBy action of more or less concentrated HCl on sucrose, glucose or fructose; hence, its reported presence in caramels.
Taste threshold valuesTaste characteristics at 70 ppm: acidic, sweet, creamy and slight dairy.
Synthesis Reference(s)Tetrahedron Letters, 30, p. 5329, 1989 DOI: 10.1016/S0040-4039(01)93778-5
Tag:Levulinic acid(123-76-2) Related Product Information
Levulinic acid ethyl,LEVULINIC ACID ETHYL ESTER,Levulinic acid ethyl ester 4-oxopentanoate Acetyl-D-2-aminobutyric acid O-Acetyl-L-carnitine hydrochloride ACETOXYPROPYLTRIMETHOXYSILANE Acetoxyacetyl chloride Acetyl tributyl citrate Acetylsalicylic acid Acetylacetone Levulinic acid, butyl ester,LEVULINIC ACID N-BUTYL ESTER Levulinic acid sodium salt Pentanoic acid, 4-oxo-, propyl ester Ferrous acetylacetonate 2,4-PENTANEDIONE, SILVER DERIVATIVE ZINC ACETYLACETONATE HYDRATE CERIUM ACETYL ACETONATE NEODYMIUM ACETYLACETONATE DYSPROSIUM 2,4-PENTANEDIONATE ERBIUM (III) 2,4-PENTANEDIONATE