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Lactic acid

Lactic acid  Structure
CAS No.
50-21-5
Chemical Name:
Lactic acid
Synonyms
2-Hydroxypropanoic acid;DL-Lactic acid;Lactic;2-HYDROXYPROPIONIC ACID;dl-lactate;Purac;actic acid;LACTIC ACID POWDER;Biolac;FEMA 2611
CBNumber:
CB8193447
Molecular Formula:
C3H6O3
Molecular Weight:
90.08
MOL File:
50-21-5.mol
MSDS File:
SDS
Modify Date:
2024/7/14 20:44:35

Lactic acid Properties

Melting point 18°C
alpha -0.05 º (c= neat 25 ºC)
Boiling point 122 °C/15 mmHg (lit.)
Density 1.209 g/mL at 25 °C (lit.)
vapor density 0.62 (vs air)
vapor pressure 19 mm of Hg (@ 20°C)
refractive index n20/D 1.4262
FEMA 2611 | LACTIC ACID
Flash point >230 °F
storage temp. 2-8°C
solubility Miscible with water and with ethanol (96 per cent).
pka 3.08(at 100℃)
form syrup
color Colorless to yellow
Specific Gravity 1.209
PH 3.51(1 mM solution);2.96(10 mM solution);2.44(100 mM solution);
Odor at 100.00 %. odorless
Odor Type odorless
Water Solubility SOLUBLE
Merck 14,5336
JECFA Number 930
BRN 1209341
Dielectric constant 22.0(16℃)
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey JVTAAEKCZFNVCJ-UHFFFAOYSA-N
LogP -0.72
CAS DataBase Reference 50-21-5(CAS DataBase Reference)
NIST Chemistry Reference Propanoic acid, 2-hydroxy-(50-21-5)
EPA Substance Registry System Lactic acid (50-21-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05
Signal word  Danger
Hazard statements  H315-H318
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P362+P364
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
HS Code  29181100
NFPA 704
1
3 1

Lactic acid price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W261114 Lactic acid natural, ≥85% 50-21-5 1SAMPLE-K ₹5347.55 2022-06-14 Buy
Sigma-Aldrich(India) W261106 Lactic acid 85%, FCC 50-21-5 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W261114 Lactic acid natural, ≥85% 50-21-5 1KG ₹7241.93 2022-06-14 Buy
Sigma-Aldrich(India) W261106 Lactic acid 85%, FCC 50-21-5 1KG ₹6971.3 2022-06-14 Buy
Sigma-Aldrich(India) W261106 Lactic acid 85%, FCC 50-21-5 25KG ₹35397.75 2022-06-14 Buy
Product number Packaging Price Buy
W261114 1SAMPLE-K ₹5347.55 Buy
W261106 1SAMPLE-K ₹5141.88 Buy
W261114 1KG ₹7241.93 Buy
W261106 1KG ₹6971.3 Buy
W261106 25KG ₹35397.75 Buy

Lactic acid Chemical Properties,Uses,Production

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.

Occurrence

Reported found in Papaver somniferum L.; it is a constituent of wine and sour milk; the two optically active isomers are found in muscular tissues and are formed by the action of lactic acid–producing bacteria in several fermentation processes. Also reported found in guava, grapes, melon, wheat bread, cheeses, yogurt, milk, cream, buttermilk, egg, cooked beef, cognac, cider, sherry, grape wine, beer, grape brandy, whiskey, cocoa, coffee, tea, mango, sake, wort, dried, bonito, cassava, Bourbon vanilla, chicory root, Cape gooseberry and cherimoya.

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.

Production Methods

Lactic acid is prepared by the fermentation of carbohydrates, such as glucose, sucrose, and lactose, with Bacillus acidi lacti or related microorganisms. On a commercial scale, whey, corn starch, potatoes, or molasses are used as a source of carbohydrate. Lactic acid may also be prepared synthetically by the reaction between acetaldehyde and carbon monoxide at 130–200°C under high pressure, or by the hydrolysis of hexoses with sodium hydroxide.
Lactic acid prepared by the fermentation of sugars is levorotatory; lactic acid prepared synthetically is racemic. However, lactic acid prepared by fermentation becomes dextrorotatory on dilution with water owing to the hydrolysis of (R)-lactic acid lactate to (S)- lactic acid.

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.

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.

Pharmaceutical Applications

Lactic acid is used in beverages, foods, cosmetics, and pharmaceuticals as an acidifying agent and acidulant.
In topical formulations, particularly cosmetics, it is used for its softening and conditioning effect on the skin. Lactic acid may also be used in the production of biodegradable polymers and microspheres, such as poly(D-lactic acid), used in drug delivery systems.
Lactic acid is also used as a food preservative. Therapeutically, lactic acid is used in injections, in the form of lactate, as a source of bicarbonate for the treatment of metabolic acidosis; as a spermicidal agent; in pessaries for the treatment of leukorrhea; in infant feeds; and in topical formulations for the treatment of warts.

Industrial uses

lactic acid showed good depressing effect on hornblende, pyroxene and biotite during flotation of hematite and ilmenite minerals.

Safety

Lactic acid occurs in appreciable quantities in the body as an end product of the anaerobic metabolism of carbohydrates and, while harmful in the concentrated form , can be considered nontoxic at the levels at which it is used as an excipient. A 1% v/v solution, for example, is harmless when applied to the skin.
There is evidence that neonates have difficulty in metabolizing (R)-lactic acid, and this isomer and the racemate should therefore not be used in foods intended for infants aged less than 3 months old.
There is no evidence that lactic acid is carcinogenic, teratogenic, or mutagenic.
LD50 (guinea pig, oral): 1.81 g/kg
LD50 (mouse, oral): 4.88 g/kg
LD50 (mouse, SC): 4.5 g/kg
LD50 (rat, oral): 3.73 g/kg

storage

Lactic acid is hygroscopic and will form condensation products such as polylactic acids on contact with water. The equilibrium between the polylactic acids and lactic acid is dependent on concentration and temperature. At elevated temperatures lactic acid will form lactide, which is readily hydrolyzed back to lactic acid.
Lactic acid should be stored in a well-closed container in a cool, dry place.

Incompatibilities

Incompatible with oxidizing agents, iodides, and albumin. Reacts violently with hydrofluoric acid and nitric acid.

Regulatory Status

GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (IM, IV, and SC injections; oral syrups and tablets; topical and vaginal preparations). Included in medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

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