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L-Lactic Acid - High purity grade, 90%, high purity , CAS No.79-33-4

In stock
Item Number
L107596
Grouped product items
SKU Size
Availability
Price Qty
L107596-25ml
25ml
3
$9.90
L107596-100ml
100ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$29.90
L107596-500ml
500ml
3
$109.90

Basic Description

Synonyms L-(+)-Lactic acid, BioXtra, >=98% (titration) | L-Milchsaeure | (S)-2-Hydroxypropanoate | (S)-2-hydroxy-Propanoate | (S)-LACTIC ACID (EP MONOGRAPH) | L-(+)-Lactic acid 95% liquid | LACTIC ACID, L-(II) | (S)-LACTIC ACID [EP MONOGRAPH] | 1-Hydroxyethane 1-c
Specifications & Purity Moligand™, high-purity, ≥90%
Biochemical and Physiological Mechanisms L-(+)-Lactic acid is used as a substrate for lactic acid dehydrogenase and lactate oxidase.
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade high-purity, Moligand™
Product Description

L-(+)-Lactic acid is the only naturally occurring lactic acid in humans and mammals. Commercially, few bacteria like Lactobacillus casei, L. delbrueckii, Streptococcus lactisproduces L-Lactic acid by fermentation process. Lactic acid activates hydroxycarboxylic acid receptor, G-protein coupled receptor 81 (GPR81).
Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Hydroxy acids and derivatives
Subclass Alpha hydroxy acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Alpha hydroxy acids and derivatives
Alternative Parents Secondary alcohols  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Alpha-hydroxy acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as alpha hydroxy acids and derivatives. These are organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon.
External Descriptors 2-hydroxypropanoic acid

Associated Targets(Human)

HCAR1 Tchem Hydroxycarboxylic acid receptor 1 (0 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
MRC5 (9203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A549 (127892 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

SARS-CoV-2 (38078 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (2S)-2-hydroxypropanoic acid
INCHI InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1
InChIKey JVTAAEKCZFNVCJ-REOHCLBHSA-N
Smiles C[C@H](O)C(O)=O
Isomeric SMILES C[C@@H](C(=O)O)O
WGK Germany 1
RTECS OD2800000
UN Number 3265
Packing Group III
Molecular Weight 90.08
Beilstein 1720251
Reaxy-Rn 1720251
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720251&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

51 results found

Lot Number Certificate Type Date Item
E2528395 Certificate of Analysis May 21, 2025 L107596
E2528394 Certificate of Analysis May 21, 2025 L107596
E2528372 Certificate of Analysis May 21, 2025 L107596
L2416635 Certificate of Analysis Nov 23, 2024 L107596
L2416642 Certificate of Analysis Nov 23, 2024 L107596
L2416639 Certificate of Analysis Nov 23, 2024 L107596
D2526050 Certificate of Analysis Nov 23, 2024 L107596
L2416643 Certificate of Analysis Nov 23, 2024 L107596
L2416637 Certificate of Analysis Nov 23, 2024 L107596
I2403512 Certificate of Analysis Aug 27, 2024 L107596
I2403514 Certificate of Analysis Aug 27, 2024 L107596
I2403511 Certificate of Analysis Aug 27, 2024 L107596
C2520220 Certificate of Analysis Aug 27, 2024 L107596
I2403510 Certificate of Analysis Aug 27, 2024 L107596
I2403515 Certificate of Analysis Aug 27, 2024 L107596
H2402070 Certificate of Analysis Aug 09, 2024 L107596
F2415226 Certificate of Analysis Jun 05, 2024 L107596
F2415229 Certificate of Analysis Jun 05, 2024 L107596
F2415230 Certificate of Analysis Jun 05, 2024 L107596
F2415280 Certificate of Analysis Jun 05, 2024 L107596
E2420075 Certificate of Analysis May 23, 2024 L107596
C2429842 Certificate of Analysis Feb 27, 2024 L107596
C2429844 Certificate of Analysis Feb 27, 2024 L107596
C2429843 Certificate of Analysis Feb 27, 2024 L107596
E2329773 Certificate of Analysis May 17, 2023 L107596
J2309056 Certificate of Analysis May 17, 2023 L107596
E2329774 Certificate of Analysis May 17, 2023 L107596
E2329781 Certificate of Analysis May 17, 2023 L107596
E2329776 Certificate of Analysis May 17, 2023 L107596
A2330208 Certificate of Analysis Dec 15, 2022 L107596
A2330172 Certificate of Analysis Dec 15, 2022 L107596
A2330019 Certificate of Analysis Dec 15, 2022 L107596
A2330096 Certificate of Analysis Dec 15, 2022 L107596
I2214068 Certificate of Analysis Aug 31, 2022 L107596
I2214069 Certificate of Analysis Aug 31, 2022 L107596
I2214070 Certificate of Analysis Aug 31, 2022 L107596
C2330626 Certificate of Analysis Aug 31, 2022 L107596
I2214071 Certificate of Analysis Aug 31, 2022 L107596
G2207317 Certificate of Analysis Jun 24, 2022 L107596
G2207249 Certificate of Analysis Jun 24, 2022 L107596
G2207316 Certificate of Analysis Jun 24, 2022 L107596
C2219312 Certificate of Analysis Mar 01, 2022 L107596
F2209144 Certificate of Analysis Mar 01, 2022 L107596
J2318750 Certificate of Analysis Mar 01, 2022 L107596
C2219413 Certificate of Analysis Mar 01, 2022 L107596
C2219306 Certificate of Analysis Mar 01, 2022 L107596
C2219527 Certificate of Analysis Mar 01, 2022 L107596
L2301088 Certificate of Analysis Mar 01, 2022 L107596
C2219528 Certificate of Analysis Mar 01, 2022 L107596
A2221075 Certificate of Analysis Jan 25, 2022 L107596
E2306070 Certificate of Analysis Sep 15, 2021 L107596

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Chemical and Physical Properties

Solubility Soluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide.
Sensitivity Moisture & Light sensitive
Refractive Index 1.4260 to 1.4310
Specific Rotation[α] -10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.)
Flash Point(°C) 110 °C
Molecular Weight 90.080 g/mol
XLogP3 -0.700
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Exact Mass 90.0317 Da
Monoisotopic Mass 90.0317 Da
Topological Polar Surface Area 57.500 Ų
Heavy Atom Count 6
Formal Charge 0
Complexity 59.100
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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