Homogentisic Acid - ≥97% , CAS No.451-13-8

CAS: 451-13-8 Cat. No.: H157029 Molecular Weight: 168.15 Beilstein Registry Number: 10407 EC Number: 207-192-7
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
AKOS004910342 | CHEBI:44747 | s9352 | Homogentisic acid | 2,5-Dihydroxyphenylacetic acid | SY051598 | Homogentisate acid | (2,5-dihydroxyphenyl)-Acetate | 2,5-Dihydroxy-benzeneacetate | 4-10-00-01506 (Beilstein Handbook Reference) | Melanic acid | T70932
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
50mg
H157029-50mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$29.90

$44.90
Save $15.00 (33.41%)
250mg
H157029-250mg
1

$111.90

$167.90
Save $56.00 (33.35%)
1g
H157029-1g
1

$300.90

$451.90
Save $151.00 (33.41%)
5g
H157029-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$739.90
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
AKOS004910342 | CHEBI:44747 | s9352 | Homogentisic acid | 2, 5-Dihydroxyphenylacetic acid | SY051598 | Homogentisate acid | (2, 5-dihydroxyphenyl)-Acetate | 2, 5-Dihydroxy-benzeneacetate | 4-10-00-01506 (Beilstein Handbook Reference) | Melanic acid | T70932
Specifications & Purity
≥97%
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%
Names and Identifiers
Pubchem Sid504750415
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750415
Canonical SmilesC1=CC(=C(C=C1O)CC(=O)O)O
IUPAC Name2-(2,5-dihydroxyphenyl)acetic acid
InChIKeyIGMNYECMUMZDDF-UHFFFAOYSA-N
INCHI1S/C8H8O4/c9-6-1-2-7(10)5(3-6)4-8(11)12/h1-3,9-10H,4H2,(H,11,12)
Isomeric SMILES C1=CC(=C(C=C1O)CC(=O)O)O
Molecular Weight 168.15
Beilstein 10407
Reaxy-Rn 2692860
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2692860&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ 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
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassPhenylacetic acids
Intermediate Tree Nodes Not available
Direct Parent2(hydroxyphenyl)acetic acids
Alternative Parents Hydroquinones  1-hydroxy-2-unsubstituted benzenoids  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents 2(hydroxyphenyl)acetic acid - Hydroquinone - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 2(hydroxyphenyl)acetic acids. These are phenylacetic acids that carry a hydroxyl group at the 2-position.
External Descriptors hydroquinones - dihydroxyphenylacetic acid
3D Structure
Interactive Chemical Structure Model





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.

14 results found

Lot NumberCertificate TypeDateItem
G2216471Certificate of AnalysisApr 07, 2026 H157029
L2505476Certificate of AnalysisDec 13, 2025 H157029
L2505477Certificate of AnalysisDec 12, 2025 H157029
K2524605Certificate of AnalysisNov 29, 2025 H157029
K2524656Certificate of AnalysisNov 25, 2025 H157029
C2527263Certificate of AnalysisMar 31, 2025 H157029
I2418365Certificate of AnalysisSep 25, 2024 H157029
I2418366Certificate of AnalysisSep 25, 2024 H157029
I2308639Certificate of AnalysisSep 16, 2023 H157029
I2308642Certificate of AnalysisSep 16, 2023 H157029
I2308651Certificate of AnalysisSep 16, 2023 H157029
I2308655Certificate of AnalysisSep 16, 2023 H157029
E2311147Certificate of AnalysisJul 21, 2022 H157029
G2216350Certificate of AnalysisJul 21, 2022 H157029

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Chemical and Physical Properties
Melt Point(°C)147 °C
Molecular Weight168.150 g/mol
XLogP30.500
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass168.042 Da
Monoisotopic Mass168.042 Da
Topological Polar Surface Area77.800 Ų
Heavy Atom Count12
Formal Charge0
Complexity168.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Shiling Liu, Siying Qin, Tengfei Zhang, Heng Zhang, Junqi Zhu, Xiaoli Li, Yuanfu Li, Feng Zhao.  (2025)  Basing target enzyme study the enantioselective bioactivity action mechanism of flusulfinam, a novel HPPD inhibitor herbicide.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:40082037] [10.1016/j.pestbp.2025.106346]
2. Wendi Xuan, Yupei Hu, Sicong Li, Xiaozhen Zhou, Meng Chen, Chenyao Wu, Xiang Gao, Gaoyan Xu, Jine Zhao, Lili Xia, Wei Feng, Yu Chen.  (2025)  Biohybrid Bacteria as Living Nanofactories for Disrupting Diabetic Wound Pathological Cascade via Antimicrobial-Regenerative Coupling.  Advanced Healthcare Materials,      [PMID:41025751] [10.1002/adhm.202503107]
3. Liu Xin, Xu Qing-qing, Zhang Yi-bo, Yuan Shi-yu, Huang Wen-li, Pi Ming-shan, Xiong Qi, Gui Yu-ran, Deng Shi-chao, Wan Ling, Xiao Yi-fan, Wang Xiao-chuan, Shu Xi-ji, Xia Yi-yuan.  (2026)  Homogentisic Acid Disrupts the Blood–Brain Barrier and Promotes Aβ Aggregation in Alzheimer’s Disease.  Current Medical Science,      [PMID:41642448] [10.1007/s11596-026-00165-0]
4. Zhu Xiangyu, Lin Jiawen, Liang Shuli, Qiu Chenyi, Jiang Yuchen, Liu Hengrui, Zhu Kun, Wang Qi, Du Chenfeng, Li Yonghao, Mao Yuanhui, Zheng Huanbin, Liu Chengan, Zhao Yeyao, An Meirong, Wu Yifeng, Liu Jun, Zhang Xinying, Lin Ying.  (2026)  Biosynthesis of pyomelanin from methanol with engineered Komagataella phaffii and its characterizations.  Nature Communications,      [PMID:] [10.1038/s41467-026-70512-1]
Solution Calculators
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