L-Lactic acid
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L-Lactic acid
structure -
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CAS No:
79-33-4
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Formula:
C3H6O3
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Chemical Name:
L-Lactic acid
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Synonyms:
Propanoic acid,2-hydroxy-,(2S)-;Lactic acid,L-;Propanoic acid,2-hydroxy-,(S)-;(2S)-2-Hydroxypropanoic acid;d-Lactic acid;Paralactic acid;Sarcolactic acid;(S)-(+)-Lactic acid;(+)-Lactic acid;L-Lactic acid;(S)-Lactic acid;L-(+)-α-Hydroxypropionic acid;Espiritin;Tisulac;(S)-2-Hydroxypropionic acid;L-(+)-Lactic acid;(S)-2-Hydroxypropanoic acid;PH 90;PURAC;PURAC Powder H 60;HiPure 90;(2S)-2-Hydroxypropanoic acid;Purac FCC 50;Purac Sanilac;1715-99-7
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CAS No:
Description
L-Lactic acid is a buildiing block which can be used as a precursor for the production of the bioplastic polymer poly-lactic acid.
Liquid
(S)-lactic acid is an optically active form of lactic acid having (S)-configuration. It has a role as an Escherichia coli metabolite and a human metabolite. It is a 2-hydroxypropanoic acid and a (2S)-2-hydroxy monocarboxylic acid. It is a conjugate acid of a (S)-lactate. It is an enantiomer of a (R)-lactic acid.|Lactic Acid, L- is the levorotatory isomer of lactic acid, the biologically active isoform in humans. Lactic acid or lactate is produced during fermentation from pyruvate by lactate dehydrogenase. This reaction, in addition to producing lactic acid, also produces nicotinamide adenine dinucleotide (NAD) that is then used in glycolysis to produce energy source adenosine triphosphate (ATP).|A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
L-Lactic acid Basic Attributes
90.08
90.08
1720251
201-196-2
F9S9FFU82N
DTXSID6034689
C61808
29181100
Characteristics
57.5
-0.7
White Powder/Solid
1.3±0.1 g/cm3
53 °C
125 °C
>230 °F
1.451
H2O: 10 mg/mL, clear, colorless
2-8°C
LD50 intraperitoneal in mouse: 3194mg/kg
-13.5 º (c=2.5, 1.5N NaOH)
Safety Information
III
8
3261
1
38-41-34-36/37/38-36-35
26-39-45-36/37/39-36
OD2800000
Xi,C
P280-P305 + P351 + P338-P310
H314
|Danger|H314 (18.87%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P332+P313, P362, P363, P405, and P501|Aggregated GHS information provided by 1172 companies from 23 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H314: Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501
L-Lactic acid Use and Manufacturing
Occurs in small quantities in the blood and muscle fluid of man and animals. The lactic acid concentration increases in muscle and blood after vigorous activity. L-(+)-Lactic acid is also present in liver, kidney, thymus gland, human amniotic fluid, and o
Pigments
Cleaning and furnishing care products
1,000,000 - 10,000,000 lb
All other chemical product and preparation manufacturing|Propanoic acid, 2-hydroxy-, (2S)-: ACTIVE
EPA Safer Chemical Functional Use Classes -> Antimicrobial Actives;Chelating Agents;Preservatives and Antioxidants;Processing Aids and Additives|Safer Chemical Classes -> Green circle - The chemical has been verified to be of low concern|Human Drugs -> EU pediatric investigation plans
Computed Properties
Molecular Weight:90.08
XLogP3:-0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:90.031694049
Monoisotopic Mass:90.031694049
Topological Polar Surface Area:57.5
Heavy Atom Count:6
Complexity:59.1
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Lactic acid from muscle tissue; may play a role in energy metabolism and regulation of muscular function.
Registered Holders
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PURAC BIOQUIMICA SAU
Active
United States
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Purac Bioquimica S.A.
Active
European Union
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R&G PharmaStudies Co., Ltd.
Inactive
China
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