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L-Lactic Acid - 80%, high purity , CAS No.79-33-4, Agonist of HCA 1 receptor
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™, ≥80%
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
Moligand™
Action Type
AGONIST
Mechanism of action
Agonist of HCA 1 receptor
Product Description
Usually used as a substrate for lactic acid dehydrogenase and lactate oxidase.
Taxonomic Classification
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
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
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)
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
Citations of This Product
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88 Citations
F2415228