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Glycolic acid - Premium-Grade Reagents ,for Analysis,, high purity , CAS No.79-14-1

In stock
Item Number
G434198
Grouped product items
SKU Size
Availability
Price Qty
G434198-100g
100g
3
$358.90

Basic Description

Synonyms DTXSID0025363 | Kyselina hydroxyoctova [Czech] | GlyPure 70 | EN300-19242 | Glycolic Acid, Crystal, Reagent | Kyselina glykolova | USEPA/OPP Pesticide Code: 000101 | CCRIS 9474 | FT-0612572 | HOCH2COOH | HO-CH2-COOH | 2-hydroxyl ethanoic acid | GLYCOLIC A
Specifications & Purity Suitable for Analysis, Premium pure
Storage Temp Room temperature
Shipped In Normal
Grade Premium pure, Suitable for Analysis

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 Monocarboxylic acids and derivatives  Carboxylic acids  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Alpha-hydroxy acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - 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 primary alcohol - 2-hydroxy monocarboxylic acid

Associated Targets(Human)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
F2 Tclin Thrombin (11687 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
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 2-hydroxyacetic acid
INCHI InChI=1S/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5)
InChIKey AEMRFAOFKBGASW-UHFFFAOYSA-N
Smiles C(C(=O)O)O
Isomeric SMILES C(C(=O)O)O
WGK Germany 1
RTECS MC5250000
UN Number 3261
Molecular Weight 76.05
Beilstein 1209322
Reaxy-Rn 1209322
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209322&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.

2 results found

Lot Number Certificate Type Date Item
G2328084 Certificate of Analysis Jul 19, 2023 G434198
G2328088 Certificate of Analysis Jul 19, 2023 G434198

Chemical and Physical Properties

Solubility water: soluble at20°C
Refractive Index 1.41
Boil Point(°C) 100°C
Melt Point(°C) 72-80°C
Molecular Weight 76.050 g/mol
XLogP3 -1.100
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Exact Mass 76.016 Da
Monoisotopic Mass 76.016 Da
Topological Polar Surface Area 57.500 Ų
Heavy Atom Count 5
Formal Charge 0
Complexity 40.200
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

Alternative Products

Citations of This Product

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53. Guojun Liu, Shaoshuai Wang, Caiming Zhou, Qiang Zhao, Jiaxue Hu, Zhenzheng Gui, Yuhui Chen, Yong Huang, Peng Zhang, Fenfen Wang.  (2024)  Boosting the activity of BiVOx via vanadium-promotion for highly selective oxidation of biomass-derived xylose toward formic acid.  FUEL,  374  (132420). 
54. Chenxi Lu, Bingqing Hu, Liangzhi Li, Xin Ju, Lishi Yan.  (2024)  Conversion of biomass-derived carbohydrates into 5-hydroxymethylfurfural over sulfonated zirconium/tin mixed-metal metal–organic frameworks in deep eutectic solvents-water based biphasic system.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,     
55. Yujie Liu, Yuting Jiang, Yan Meng, Weini Xiong, Ziling Yuan, Ruihua Liu, Chao Yang.  (2025)  Creating a multifunctional degrader for co-mineralization of p-nitrophenol and 1,2-dichloroethane and its application in wastewater bioremediation.  JOURNAL OF HAZARDOUS MATERIALS,  488  (137417). 
56. Kai Nie, Boya Li, Pixiang Wang, Yan Song, Haoxi Ben, Guangting Han, Wei Jiang, Arthur Ragauskas.  (2024)  Efficient fractionation of kenaf chemical components by using recyclable acidic DES.  INDUSTRIAL CROPS AND PRODUCTS,  211  (118239). 
57. Hejuan Wu, Hongrui Guo, Boxiong Shen, Xiao Zhang, Feng Shen.  (2025)  Enhanced glucose conversion to formic acid with deep eutectic solvents-mediated bimetallic oxides: Morphology and valence state regulation.  BIOMASS & BIOENERGY,  194  (107698). 
58. Yuanming Feng, Yunpeng Bi, Yifei Wang, Fang Yang, Guangxing Yang, Yuguang Jin, Xiaoyue Wan, Yihu Dai, Yanhui Yang, Dan Yang, Chunmei Zhou.  (2025)  Enhanced Glycerol Oxidation Toward Dihydroxyacetone Over Gold/Palladium Binary Nanocatalysts by Structure Control.  CHEMISTRY-A EUROPEAN JOURNAL,    (e202500601). 
59. Kaiqiang Cheng, Zhengli Zhang, Ruirui Cui, Yi Wang, Mi Hu, Yong Deng, Shaolu Chen, Junli Li.  (2024)  Glycolic Acid Doped PFN-Br as Cathode Interface to Achieve High-Efficiency in Organic Solar Cells.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,    (135485). 
60. Jianbo Xin, Yue Gao, Chenghao Zhang, Le Yang, Sushi Liu, Ke Li, Minghao Zhou, Yang Liu, Jing Zhang, William Cai.  (2024)  High performance Cu sintering joint for power devices enabled by in-situ generation of Cu particles with multi-level hierarchical structures.  JOURNAL OF MATERIALS PROCESSING TECHNOLOGY,  329  (118435). 
61. Tao Sun, Ying Li, Yangyang Wang, Qing Yang, Jiahui Du, Jian Hu, Sarula, Tungalag Dong, Xueyan Yun.  (2024)  High performance poly(L-lactic acid)-based film by one-step synthesis of poly (L-lactic acid-co-butylene itaconate-co-glycolic acid) for efficient preservation of yogurt storage.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  268  (131746). 
62. Xing Wei, Qingqiang Wang, Xunli Zhang, Ying Chen, Nan Jin, Yuchao Zhao.  (2024)  Highly selective oxidation of glucose to formic acid and exploring reaction pathways using continuous flow microreactors.  FUEL,  372  (132198). 
63. Fengyi Zhou, Dingyi Shi, Wenbo Mu, Shao Wang, Zeyu Wang, Chenyang Wei, Ruiqi Li, Tiancheng Mu.  (2024)  Machine learning models accelerate deep eutectic solvent discovery for the recycling of lithium-ion battery cathodes.  GREEN CHEMISTRY,  26  (13): (7857-7868). 
64. Lunfei Zou, Yao Wang, Xingdan Wang, Xiaoqiu Yang, Qiwei Zhang, Qi Zheng.  (2024)  Stable isotope labeling-based two-step derivatization strategy for analysis of Phosphopeptides.  Journal of Proteomics,  297  (105128). 
65. Xiaoyuan Liu, Yu Zou, Jiang Jiang.  (2024)  Sunlight-driven selective oxidation of glycerol on formate oxidase mimicking AuPt/TiO2.  APPLIED CATALYSIS B-ENVIRONMENTAL,  350  (123927). 
66. Yongming Xu, Wenzhao Liu, Bo Xu, Ke Wang, Jinchu Yang, Yueqi Si, Xuebin Zhao, Tingting Zhang, Zhan Zhang, Xueyi Qiao, Tianliang Lu.  (2024)  Synthesis of glycolic acid by selective oxidation of ethylene glycol over Pt/Sn-Beta in a base-free medium.  Reaction Chemistry & Engineering,     
67. Zhonglei Meng, Rongxiu Qin, Rusi Wen, Junkang Xie, Guiqing Li, Yonghong Zhou.  (2024)  Synthesis of terpinyl acetate from α-pinene catalyzed by α-hydroxycarboxylic acid–boric acid composite catalyst.  PLoS One,  19  (4): (e0299218). 
68. Shuai Liu, Baocheng Chen, Yuhan Wang, Hui Wang, Xu Cheng, Haibo Wang, Jinghong Qiu, Zongliang Du.  (2024)  Ultrastrength High-Sensitivity Poly(acrylic acid)-Based Deep Eutectic Solvents Gel for Wearable Strain Sensing and Human Health Monitoring.  ACS Applied Polymer Materials,  (9): (5385-5393). 

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