4-Hydroxybenzyl Alcohol - 10mM in DMSO , CAS No.623-05-2

CAS: 623-05-2 Cat. No.: H425157 Formula: C7H8O2 Peso molecolare: 124.14 Beilstein Registry Number: 1858967 Numero EC: 210-768-0
Disponibile su ordine
GRADE & PURITY 10mM in DMSO
Synonyms
DTXSID8073920 | HMS3885O08 | 4-Hydroxybenzylalcohol | 4-Hydroxy-benzylalcohol | 4-hydroxybenzyl-alcohol | Benzenemethanol, 4-hydroxy- (9CI) | EC 210-768-0 | SCHEMBL62690 | STL284640 | EINECS 210-768-0 | p-Hydroxybenzyl alcohol | p-hydroxy-Benzyl alcohol |
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Germania (EU)
USA*
Price
Qty
1ml
H425157-1ml
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1 Disponibile
23,34€
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 22 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

4-Hydroxybenzyl alcohol (HBA) is a phenolic compound found in Gastrodia elata. It is as an antioxidant and anti-asthmatic agent.

4-Hydroxybenzyl alcohol can be used as a precursor for the synthesis of:

• HBA-incorporated copolyoxalate (HPOX) nanoparticles as potential drug delivery system.

• Poly(4-hydroxybenzyl alcohol) by enzyme catalyzed reaction.

• 4-Hydroxybenzyl imidazole derivatives.

Specifications

Sinonimi
DTXSID8073920 | HMS3885O08 | 4-Hydroxybenzylalcohol | 4-Hydroxy-benzylalcohol | 4-hydroxybenzyl-alcohol | Benzenemethanol, 4-hydroxy- (9CI) | EC 210-768-0 | SCHEMBL62690 | STL284640 | EINECS 210-768-0 | p-Hydroxybenzyl alcohol | p-hydroxy-Benzyl alcohol |
Specifiche e purezza
10mM in DMSO
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori
Pubchem Sid528771482
Sorrisi canoniciC1=CC(=CC=C1CO)O
IUPAC Name4-(hydroxymethyl)phenol
InChIKeyBVJSUAQZOZWCKN-UHFFFAOYSA-N
INCHI1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2
Isomeri SMILES C1=CC(=CC=C1CO)O
WGK Germania 3
Peso molecolare 124.14
Beilstein 1858967
Reaxy-Rn 1858967
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1858967&ln=

Documentazione

📋 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
ClasseBenzene and substituted derivatives
SubclassBenzyl alcohols
Intermediate Tree Nodes Not available
Direct ParentBenzyl alcohols
Alternative Parents 1-hydroxy-2-unsubstituted benzenoids  Primary alcohols  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzyl alcohol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzyl alcohols. These are organic compounds containing the phenylmethanol substructure.
External Descriptors a phenol
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TOP1 Tclin DNA topoisomerase I (7553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABAT Tclin Gamma-amino-N-butyrate transaminase (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH5A1 Tclin Succinate semialdehyde dehydrogenase (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FYN Tclin Tyrosine-protein kinase FYN (5308 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RKO (1376 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SGC-7901 (2773 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KB (17409 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CRK Tchem Proto-oncogene C-crk (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT-CO2 Tchem Cytochrome c oxidase subunit 2 (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HGC-27 (1452 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Grb2 Growth factor receptor-bound protein 2 (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
B16-F10 (4610 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
SensibilitàAir & Light & Heat sensitive
Punto di ebollizione (°C)251-253°C
Punto di fusione (°C)114-122°C
Peso molecolare124.140 g/mol
XLogP30.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass124.052 Da
Monoisotopic Mass124.052 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity75.000
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
Riferimenti
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4. Hongjie Zhang, Weijian Chen, Jing Wang, Wenxiang Du, Bibo Wang, Lei Song, Yuan Hu, Xiaopeng Ma.  (2022)  A novel ROS-activable self-immolative prodrug for tumor-specific amplification of oxidative stress and enhancing chemotherapy of mitoxantrone.  BIOMATERIALS,      [PMID:36538847] [10.1016/j.biomaterials.2022.121954]
5. Peng Xie, Wang Zhang, Wugao Wu, Zhuanglin Shen, Mingliang Wang, Yuxiao Lai, Yantao Chen, Zhongfan Jia.  (2022)  Phenoxyl mediators improve enzymatic degradation of organic pollutants: Effect and mechanism.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:35750102] [10.1016/j.ijbiomac.2022.06.124]
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8. Shouhua Su, Juan Wang, Chao Li, Jinfeng Yuan, Zhicheng Pan, Mingwang Pan.  (2021)  Short-Branched Fluorinated Polyurethane Coating Exhibiting Good Comprehensive Performance and Potential UV Degradation in Leather Waterproofing Modification.  Coatings,  11  (4): (395).  [PMID:] [10.3390/coatings11040395]
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10. Yin Hua, Hu Tiandong, Zhuang Yibin, Liu Tao.  (2020)  Metabolic engineering of Saccharomyces cerevisiae for high-level production of gastrodin from glucose.  Microbial Cell Factories,  19  (1): (1-12).  [PMID:33243241] [10.1186/s12934-020-01476-0]
11. Limin Li, Bin Hao, Yulong Zhang, Shen Ji, Guixin Chou.  (2020)  Metabolite Profiling and Distribution of Militarine in Rats Using UPLC-Q-TOF-MS/MS.  MOLECULES,  25  (5): (1082).  [PMID:32121087] [10.3390/molecules25051082]
12. Yun-Xiao Zhang, Peng Zeng, Yu-Xiang Yu, Wei-De Zhang.  (2019)  Integration of nickel complex as a cocatalyst onto in-plane benzene ring-incorporated graphitic carbon nitride nanosheets for efficient photocatalytic hydrogen evolution.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.122635]
13. Dong Shihao, Wen Ping, Zhang Qi, Li Xinyu, Tan Ken, Nieh James.  (2017)  Resisting majesty: Apis cerana, has lower antennal sensitivity and decreased attraction to queen mandibular pheromone than Apis mellifera.  Scientific Reports,  7  (1): (1-10).  [PMID:28294146] [10.1038/srep44640]
14. Yanfen Bai, Hua Yin, Huiping Bi, Yibin Zhuang, Tao Liu, Yanhe Ma.  (2016)  De novo biosynthesis of Gastrodin in Escherichia coli.  METABOLIC ENGINEERING,      [PMID:26804288] [10.1016/j.ymben.2016.01.002]
15. Jingying Pan, Jie Fu, Shuguang Deng, Xiuyang Lu.  (2015)  Distribution coefficient of products from lignin oxidative degradation in organic-water systems.  FUEL PROCESSING TECHNOLOGY,      [PMID:] [10.1016/j.fuproc.2015.09.016]
16. Jingying Pan, Jie Fu, Xiuyang Lu.  (2015)  Microwave-Assisted Oxidative Degradation of Lignin Model Compounds with Metal Salts.  ENERGY & FUELS,      [PMID:] [10.1021/acs.energyfuels.5b00735]
17. Mo Qiwen, Yuan Jifeng.  (2024)  Minimal aromatic aldehyde reduction (MARE) yeast platform for engineering vanillin production.  Biotechnology for Biofuels and Bioproducts,  17  (1): (1-12).  [PMID:38184607] [10.1186/s13068-023-02454-5]
18. Zhu Jianfei, Tian Dongling, Chen Xiaomei, Huang Tingting, Chen Xi.  (2024)  Preparation of Chitosan-phenolic Aldehyde Fragrance Oleogels and Comparative Study of their Structure and Properties.  Food and Bioprocess Technology,      [PMID:] [10.1007/s11947-024-03390-4]
19. Sheng Lin, Xia Cheng, Xiyi Chen, Jinxuan He, Wenxiu An, Qiufang Bai, Qixian Chen, Lie Ma, Jianhua Hu, Yue Wang, Xiabin Lan.  (2025)  Synthetic Redox-Responsive Nanocomplexes Facilitate Spatially Controlled mRNA Release and Tumor-Selective Expression.  BIOCONJUGATE CHEMISTRY,      [PMID:40634257] [10.1021/acs.bioconjchem.5c00264]
20. Rui Zhang, Danhua Mao, Yiyong Fu, Rong Ju, Guoqing Wei.  (2025)  A self-assembled and H2O2-activatable hybrid nanoprodrug for lung infection and wound healing therapy.  Theranostics,  15  (12): (5953).  [PMID:40365280] [10.7150/thno.114344]
21. Tianyin Huang, Yifan Yu, Wentao Zhang, Yue Zhao, Yiliang Tao, Wenguang Huang, Bingdang Wu.  (2026)  Molecular orbital-guided design of laccase–mediator systems for antibiotic removal in the presence of humic acid.  BIORESOURCE TECHNOLOGY,      [PMID:41513177] [10.1016/j.biortech.2026.133957]
22. Xinyue Zhao, Naijie Wei, Ziyang Fang, Yingyan Xie, Xiaowen Yan, Qiuquan Wang.  (2026)  A Targeted Covalently Activated Chemotherapy Strategy Synergistically Enhances Cytotoxicity of Ibrutinib and Selectivity of Doxorubicin to B-cell Lymphoma Cells.  JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:41615077] [10.1021/acs.jmedchem.5c02215]
23. Haiyang Xie, Yuhan Chen, Xianni Li, Xiaoling Lu, Hao Lin, Yanjuan Zhang, Zuqiang Huang, Huayu Hu, Tao Gan.  (2026)  Atomically dispersed manganese catalysts with electron-deficient Mn–N2O2 sites to enhance the selective oxidation of benzyl alcohol to benzaldehyde via PMS-based non-radical oxidation pathway.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2026.139849]
24. Yong Wang, Yongyao Li, Zhongjun Cheng, Caiyun Wang, Min Liu, Maochang Zhou, Xiangyu Zhang.  (2026)  Seed Weight and Seeding Rate of Gastrodia elata Bl. f. glauca S. Chow: Significant Yield Increase but Limited Effect on Bioactive Components.  Forests,  17  (8): (956).  [PMID:] [10.3390/f17080956]
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