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2-hydroxypropanoic acid

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Origin: China

Cas No: 50-21-5

Specification: 99%min

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    CAS No.: 50-21-5 Formula: C3H6O3 Molecular Weight: 90.07790

    Description

    Lactic acid is an organic compound with the formula CH3CH(OH)CO2H. In its solid state, it is white and water-soluble. In its liquid state, it is clear. It is produced both naturally and synthetically. With a hydroxyl group adjacent to the carboxyl group, lactic acid is classified as an alpha-hydroxy acid (AHA). In the form of its conjugate base called lactate, it plays a role in several biochemical processes.
    In solution, it can ionize a proton from the carboxyl group, producing the lactate ion CH 3CH(OH)CO− 2. Compared to acetic acid, its pKa is 1 unit less, meaning lactic acid deprotonates ten times more easily than acetic acid does. This higher acidity is the consequence of the intramolecular hydrogen bonding between the α-hydroxyl and the carboxylate group.
    Lactic acid is chiral, consisting of two optical isomers. One is known as L-(+)-lactic acid or (S)-lactic acid and the other, its mirror image, is D-(−)-lactic acid or (R)-lactic acid. A mixture of the two in equal amounts is called DL-lactic acid, or racemic lactic acid.
    Lactic acid is hygroscopic. DL-lactic acid is miscible with water and with ethanol above its melting point which is around 17 or 18°C. D-lactic acid and L-lactic acid have a higher melting point.
    In animals, L-lactate is constantly produced from pyruvate via the enzyme lactate dehydrogenase (LDH) in a process of fermentation during normal metabolism and exercise. It does not increase in concentration until the rate of lactate production exceeds the rate of lactate removal, which is governed by a number of factors, including monocarboxylate transporters, concentration and isoform of LDH, and oxidative capacity of tissues. The concentration of blood lactate is usually 1–2 mmol/L at rest, but can rise to over 20mmol/L during intense exertion and as high as 25mmol/L afterward.
    In industry, lactic acid fermentation is performed by lactic acid bacteria, which convert simple carbohydrates such as glucose, sucrose, or galactose to lactic acid. These bacteria can also grow in the mouth; the acid they produce is responsible for the tooth decay known as caries.
    In medicine, lactate is one of the main components of lactated Ringer's solution and Hartmann's solution. These intravenous fluids consist of sodium and potassium cations along with lactate and chloride anions in solution with distilled water, generally in concentrations isotonic with human blood. It is most commonly used for fluid resuscitation after blood loss due to trauma, surgery, or burns.

    Basic Info

    Chemical Name 2-hydroxypropanoic acid
    Synonyms

    2-Hydroxypropionic acid;
    DL-Lactic acid;
    1H-Pyrrolo[2,3-b]pyridine-3-acetic acid, 5-bromo-a-oxo-;
    Lactic acid;

    CAS No. 50-21-5
    Molecular Formula C3H6O3
    Molecular Weight 90.07790
    PSA 57.53000
    LogP -0.54820

    Properties

    Appearance & Physical State colourless to yellow liquid
    Density 1.276 g/cm3
    Boiling Point 227.6ºC at 760 mmHg
    Melting Point 18ºC
    Flash Point 109.9ºC
    Refractive Index 1.4252-1.4272
    Stability Stable. Combustible. Incompatible with strong oxidizing agents.
    Storage Condition 2-8ºC

    Safety Info

    RTECS OD2800000
    Hazard Class 8
    Safety Statements 26-39-45-36/37/39
    HS Code 2918110000
    WGK Germany 2
    Packing Group III
    RIDADR UN 1760
    Risk Statements R34; R38; R41
    Hazard Codes Xi; C
    Signal Word Danger
    Hazard Declaration H315; H318
    Symbol GHS05
    Caution Statement P280; P305 + P351 + P338

    Synthesis Route

    2-hydroxy-3-((2-hydroxyethyl)thio)propanoic acid2-hydroxypropanoic acid+2-hydroxypropanoic acid
    N<sup>5</sup>-((2R)-1-((carboxymethyl)amino)-3-((3-(ethylthio)-2-hydroxy-3-oxopropyl)thio)-1-oxopropan-2-yl)glutamine2-hydroxypropanoic acid+2-hydroxypropanoic acid
    sodium pyruvate2-hydroxypropanoic acid+2-hydroxypropanoic acid

    Toxicity

    Exposure Route Type of Test Species Observed Dose/Duration Toxic Effects
    Administration onto the skin Standard Draize test Rodent - rabbit 5 mg/24H -
    Administration into the eye Standard Draize test Rodent - rabbit 750 ug -
    Oral LD50 - Lethal dose, 50 percent kill Rodent - rat 3543 mg/kg 1.Details of toxic effects not reported other than lethal dose value

    Precursor

    2-hydroxy-3-((2-hydroxyethyl)thio)propanoic acid
    sodium pyruvate
    N<sup>5</sup>-((R)-1-((carboxymethyl)amino)-3-(((R)-2-hydroxypropanoyl)thio)-1-oxopropan-2-yl)-L-glutamine
    N<sup>5</sup>-((2R)-1-((carboxymethyl)amino)-3-((3-(ethylthio)-2-hydroxy-3-oxopropyl)thio)-1-oxopropan-2-yl)glutamine

    Downstream Product

    (R)-2-Chloropropanoic Acid

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