L-Lactic Acid - Moligand™, ≥95%(T) , CAS No.79-33-4

CAS: 79-33-4 Cat. No.: L639890 Formula: C3H6O3 Molecular Weight: 90.08 Beilstein Registry Number: 1720251 EC Number: 201-196-2
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥95%(T)
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
Storage
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
★
Size
Germany (EU)
USA*
Price
Qty
5g
L639890-5g
Made to order · 8–12 wks
€99.70
25g
L639890-25g
—
4 In stock
€347.88
100g
L639890-100g
—
1 In stock
€937.94
250g
L639890-250g
—
1 In stock
€2,065.13
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥95%(T) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 125 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.

Specifications

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™, ≥95%(T)
Storage
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Purity
≥95%(T)
Names and Identifiers
Pubchem Sid
Canonical Smiles
C[C@H](O)C(O)=O
IUPAC Name
(2S)-2-hydroxypropanoic acid
InChIKey
JVTAAEKCZFNVCJ-REOHCLBHSA-N
INCHI
1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1
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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

<<<<<<< HEAD Download SDS → ======= Download SDS → >>>>>>> release248-p3

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassHydroxy acids and derivatives
SubclassAlpha hydroxy acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAlpha hydroxy acids and derivatives
Alternative Parents Secondary alcohols  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
HCAR1 Tchem Hydroxycarboxylic acid receptor 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A3 Tchem Monocarboxylate transporter 4 (196 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

9 results found

Lot NumberCertificate TypeDateItem
C2401347C2401347Certificate of AnalysisMar 12, 2024 L639890
C2401348C2401348Certificate of AnalysisMar 12, 2024 L639890
C2401349C2401349Certificate of AnalysisMar 12, 2024 L639890
C2401350C2401350Certificate of AnalysisMar 12, 2024 L639890
C2401351C2401351Certificate of AnalysisMar 12, 2024 L639890
C2401352C2401352Certificate of AnalysisMar 12, 2024 L639890
C2617123C2617123Certificate of AnalysisMar 12, 2024 L639890
H2618190H2618190Certificate of AnalysisMar 12, 2024 L639890
K2506102K2506102Certificate of AnalysisMar 12, 2024 L639890
Chemical and Physical Properties
SolubilitySoluble in water (100 mg/ml), alcohol, acetone, and methanol. Insoluble in chloroform, petroleum, ether, and carbon disulfide.
SensitivityMoisture & Light sensitive
x_refractive_index1.4260 to 1.4310
x_specific_rotation-10.0 to -15.0 deg(C=2.5, 1.5mol/L NaOH sol.)
x_flash_point_drop_centigrade110 °C
x_boil_point_char122 °C/20 hPa
x_melt_point_char18 °C
Molecular Weight90.080 g/mol
XLogP3-0.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass90.0317 Da
Monoisotopic Mass90.0317 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count6
Formal Charge0
Complexity59.100
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Citations of This Product
Solution Calculators
Reviews

Customer Reviews

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