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(S)-lactic acid

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Origin: China

Cas No: 79-33-4

Specification: 99%min

Min order Quantity: 1 /kg

Supply Ability: 100 mt/month

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  • Products Specification
  • Product Description
  • Quick Details

    CAS No.:
    79-33-4
    Other Names:
    L Lactic acid
    MF:
    C3H6O3
    EINECS No.:
    201-196-2
    Place of Origin:
    China
    Type:
    Sweeteners
    Brand Name:
    ZHONGLAN
    Model Number:
    ZLSCH 201-196-2
    Product name:
    L Lactic acid
    Other name:
    L(+)-Lactic acid
    Melting point:
    52-54℃
    Boiling point:
    125℃
    Density:
    1.206
    Flash point:
    >230℉
    Color:
    colorless to yellowish
    Water solubility:
    Soluble
    COA:
    Availble
    Sample:
    Availble

    Packaging&Delivery

    Packaging Details
    25 kgs drum
    Port
    Shanghai
  • Property

    CAS No.: 79-33-4 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 (S)-lactic acid
    Synonyms

    Propanoic acid, 2-hydroxy-, (S)-;
    L-(+)-Lactic acid;
    L(+)-Lactic acid;

    CAS No. 79-33-4
    Molecular Formula C3H6O3
    Molecular Weight 90.07790
    PSA 57.53000
    LogP -0.54820

    Properties

    Appearance & Physical State crystalline solid
    Density 1.206
    Boiling Point 125ºC
    Melting Point 52-54ºC
    Flash Point 109.9ºC
    Refractive Index 1.426-1.428
    Water Solubility SOLUBLE
    Storage Condition 2-8ºC

    Safety Info

    RTECS OD2800000
    Hazard Class 8
    Safety Statements S26-S36/37/39-S45
    HS Code 2918110000
    Packing Group III
    WGK Germany 1
    RIDADR UN 3261
    Risk Statements R34
    Hazard Codes C
    Symbol GHS05
    Signal Word Danger
    Caution Statement P280; P305 + P351 + P338 + P310
    Hazard Declaration H315; H318

    Synthesis Route

    citric acidoxaloacetic acid+(S)-lactic acid
    citric acidoxaloacetic acid+(S)-lactic acid
    carbon dioxide+acetaldehyde(S)-lactic acid+Pyruvic acid

    GC Analysis

    Column type Active phase Temperature (°C) Retention Index (I) Temperature Control Method
    Capillary RTX-Wax - 2159. temperature ramp

    Precursor

    L-alanine
    (S)-Propyl 2-hydroxypropanoate
    methyl (S)-lactate
    (1S,4S)-4-(3,4-dichlorophenyl)-N-methyl-1,2,3,4-tetrahydronaphthalen-1-amine (S)-2-hydroxypropanoate

    Downstream Product

    (S)-(+)-1,2-Propanediol
    (3S,6S)-(-)-3,6-Dimethyl-1,4-Dioxane-2,5-Dione
    (3R,6S)-3,6-Dimethyl-1,4-dioxane-2,5-dione
    (S)-(-)-2-ACETOXYPROPIONYL CHLORIDE

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