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Postion:Product Catalog >API>Synthetic Anti-infective Drugs>Antiseptics & Disinfectants Drugs> Lactic acid
	Lactic acid
  • 	Lactic acid

Lactic acid

Price $1
Package 1kg
Min. Order: 1kg
Supply Ability: 100KG
Update Time: 2019-07-06

Product Details

Product Name: Lactic acid CAS No.: 50-21-5
Min. Order: 1kg Purity: 99%
Supply Ability: 100KG Release date: 2019/07/06

AD68

Lactic acid Basic information
Product Name: Lactic acid
Synonyms: FEMA 2611;DL-ALPHA-HYDROXYPROPIONIC ACID;(+/-)-LACTIC ACID;LACTIC ACID;LACTIC ACID, RACEMIC;2-HYDROXYPROPIONIC ACID, RACEMIC;(+/-)-2-HYDROXYPROPIONIC ACID;2-HYDROXYPROPIONIC ACID
CAS: 50-21-5
MF: C3H6O3
MW: 90.08
EINECS: 200-018-0
Product Categories: FOOD ADDITIVES;Plant Growth Regulator;Food & Feed ADDITIVES;ACS GradeChiral Building Blocks;Carboxylic Acids;Essential Chemicals;Organic Building Blocks;Routine Reagents;Food & Flavor Additives;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Food additive and acidulant
Mol File: 50-21-5.mol
Article illustration
 
Lactic acid Chemical Properties
Melting point  18°C
Boiling point  122 °C15 mm Hg(lit.)
alpha  -0.05 º (c= neat 25 ºC)
density  1.209 g/mL at 25 °C
refractive index  n20/D 1.4262
FEMA  2611 | LACTIC ACID
Fp  >230 °F
storage temp.  2-8°C
solubility  Miscible with water and with ethanol (96 per cent).
form  syrup
pka 3.08(at 100℃)
color  Colorless to yellow
Water Solubility  SOLUBLE
Merck  14,5336
BRN  1209341
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference 50-21-5(CAS DataBase Reference)
NIST Chemistry Reference Propanoic acid, 2-hydroxy-(50-21-5)
EPA Substance Registry System Propanoic acid, 2-hydroxy-(50-21-5)
 
Safety Information
Hazard Codes  Xi,C
Risk Statements  38-41-34-37/38
Safety Statements  26-39-45-36/37/39
RIDADR  3265
WGK Germany  2
RTECS  OD2800000
3
TSCA  Yes
HazardClass  8
PackingGroup  III
Hazardous Substances Data 50-21-5(Hazardous Substances Data)
MSDS Information
Provider Language
2-Hydroxypropanoic acid English
ACROS English
SigmaAldrich English
ALFA English
 
Lactic acid Usage And Synthesis
Chemical Properties Lactic acid, CH3CHOHCOOH, also known as 2-hydroxypropanoic acid, is a hygroscopic liquid that exists in three isometric forms. I-lactic acid is found in blood and animal tissue as a product of glucose and glycogen metabolism. d-Iactic acid is obtained by fermentation of sucrose (corn refining), The racemic mixture is present in foods prepared by bacterial fermentation or prepared synthetically. Lactic acid is soluble in water,alcohol,and ether. It is used as a solvent, in manufacturing confectionery, and in medicine.
Uses Prostaglandin E1 analogue
Uses lactic acid (sodium lactate) is a multi-purpose ingredient used as a preservative, exfoliant, moisturizer, and to provide acidity to a formulation. In the body, lactic acid is found in the blood and muscle tissue as a product of the metabolism of glucose and glycogen. It is also a component of the skin’s natural moisturizing factor. Lactic acid has better water intake than glycerin. Studies indicate an ability to increase the water-retention capacity of the stratum corneum. They also show that the pliability of the stratum corneum layer is closely related to the absorption of lactic acid; that is, the greater the amount of absorbed lactic acid, the more pliable the stratum corneum layer. Researchers report that continuous use of preparations formulated with lactic acid in concentrations ranging between 5 and 12 percent provided a mild to moderate improvement in fine wrinkling and promote softer, smoother skin. Its exfoliating properties can help in the process of removing excess pigment from the surface of the skin, as well as improving skin texture and feel. Lactic acid is an alpha hydroxy acid occurring in sour milk and other lesser-known sources, such as beer, pickles, and foods made through a process of bacterial fermentation. It is caustic when applied to the skin in highly concentrated solutions.
Definition ChEBI: A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
General Description A colorless to yellow odorless syrupy liquid. Corrosive to metals and tissue. Used to make cultured dairy products, as a food preservative, and to make chemicals.
Air & Water Reactions Soluble in water.
Reactivity Profile Lactic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Lactic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. Slowly corrodes most metals [USCG, 1999].
Health Hazard Inhalation of mist causes coughing and irritation of mucous membranes. Ingestion, even of diluted preparations, has a corrosive effect on the esophagus and stomach. Contact with more concentrated solutions can cause severe burns of skin or eye.
Fire Hazard Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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  • Address: No.967,15th Floor,Unit 7, Building 1, No.70 of DianChang Road, High-tech Development Zone, Zhengzho
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