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3-Hydroxyphenylacetic acid - 10mM in DMSO, high purity , CAS No.621-37-4

    Grade & Purity:
  • 10mM in DMSO
  • Cas Number:  621-37-4
  • Molecular Weight:  152.15
  • PubChem CID: 12122
In stock
Item Number
H425145
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H425145-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$62.90

Basic Description

Synonyms 3-Hydroxyphenylacetic acid | 621-37-4 | 2-(3-hydroxyphenyl)acetic acid | (3-Hydroxyphenyl)acetic acid | 3-Hydroxybenzeneacetic acid | (m-Hydroxyphenyl)acetic acid | Benzeneacetic acid, 3-hydroxy- | M-HYDROXYPHENYLACETIC ACID | 3-Hydroxyphenylacetate | Acetic acid, (m-hydro
Specifications & Purity 10mM in DMSO
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

3-Hydroxyphenylacetic Acid (cas# 621-37-4) is a compound useful in organic synthesis

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Phenols
Subclass 1-hydroxy-4-unsubstituted benzenoids
Intermediate Tree Nodes Not available
Direct Parent 1-hydroxy-4-unsubstituted benzenoids
Alternative Parents 1-hydroxy-2-unsubstituted benzenoids  Benzene and substituted derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aromatic homomonocyclic compounds
Substituents 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position.
External Descriptors monocarboxylic acid - phenols

Associated Targets(Human)

CAMK2A Tchem CaM kinase II alpha (1938 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Gamma-hydroxybutyrate receptor (68 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HT-22 (3261 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Gabrp GABA-A receptor; anion channel (5731 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 2-(3-hydroxyphenyl)acetic acid
INCHI InChI=1S/C8H8O3/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChIKey FVMDYYGIDFPZAX-UHFFFAOYSA-N
Smiles C1=CC(=CC(=C1)O)CC(=O)O
Isomeric SMILES C1=CC(=CC(=C1)O)CC(=O)O
WGK Germany 3
Molecular Weight 152.15
Reaxy-Rn 2086506
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2086506&ln=

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

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

Chemical and Physical Properties

Melt Point(°C) 129-133°C
Molecular Weight 152.150 g/mol
XLogP3 0.900
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 152.047 Da
Monoisotopic Mass 152.047 Da
Topological Polar Surface Area 57.500 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 144.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
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

1. Bing Wang, RuiQing Zhang, HuiYong Chen, Zhuo Li, EnZhou Liu, HaiXia Ma, Bo Zhou, Hong Hao, LinYu Jiao.  (2023)  Construction of supramolecular S-scheme heterojunctions assisted by hydrogen bond subtle-tuning actuates highly efficient photocatalytic oxidation.  CHEMICAL ENGINEERING JOURNAL,  473  (145290). 
2. Xinyi Zhang, Jiakun Zhou, Zemin Li, Yimin Qin, Ruitao Yu, Huaiwei Zhang, Yuhong Zheng, Jiangwei Zhu, Demeng Zhang, Li Fu.  (2019)  The Qualitative Electrochemical Determination of Multiple Components in Seaweed Fertilizer.  International Journal of Electrochemical Science,  14  (6283). 
3. Hui-Ying Wang, Cheng Qu, Meng-Ning Li, Chao-Ran Li, Run-Zhou Liu, Zifan Guo, Ping Li, Wen Gao, Hua Yang.  (2022)  Time-Series-Dependent Global Data Filtering Strategy for Mining and Profiling of Xenobiotic Metabolites in a Dynamic Complex Matrix: Application to Biotransformation of Flavonoids in the Extract of Ginkgo biloba by Gut Microbiota.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  70  (45): (14386–14394). 

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