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(±)-1-Phenyl-1，2-ethanediol - 98%, high purity , CAS No.93-56-1

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(±)-1-Phenyl-1，2-ethanediol - 98%, high purity , CAS No.93-56-1

3 Citations

COA

Grade & Purity:

≥98%

Cas Number: 93-56-1
Molecular Weight: 138.16
Beilstein Registry Number: 1306723
EC Number: 202-258-1
MDL number: MFCD00003546
PubChem CID: 7149
PubChem SID: 488180313

In stock

Item Number

P112689

Grouped product items
SKU	Size	Availability	Price
P112689-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$9.90
P112689-5g	5g	5	$29.90
P112689-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$45.90
P112689-25g	25g	3	$87.90
P112689-100g	100g	1	$314.90

View related series

alcohol (850) Metabolite (5307) Non heterocyclic block (8163)

Basic Description

Synonyms	AKOS004903345 \| FT-0604449 \| alpha,beta-Dihydroxyethylbenzene \| Phenylethanediol \| MFCD00003546 \| Styrolyl alcohol \| 2-phenyl-2-hydroxyethanol \| SY017543 \| CAS-93-56-1 \| 1-Phenyl-1,2-ethanediol, 97% \| 1-Phenyl-1,2-ethanediol \| Phenylethane-1,2-diol \| .alp
Specifications & Purity	≥98%
Storage Temp	Desiccated
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Benzene and substituted derivatives
Alternative Parents	Secondary alcohols 1,2-diols Primary alcohols Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Monocyclic benzene moiety - Secondary alcohol - 1,2-diol - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

HT-29 (80576 Activities)

Explore this target

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

Pubchem Sid	488180313
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180313
IUPAC Name	1-phenylethane-1,2-diol
INCHI	InChI=1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
InChIKey	PWMWNFMRSKOCEY-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)C(CO)O
Isomeric SMILES	C1=CC=C(C=C1)C(CO)O
WGK Germany	3
RTECS	KI2500000
Molecular Weight	138.16
Beilstein	1306723
Reaxy-Rn	1306723
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1306723&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.

12 results found

Lot Number	Certificate Type	Date	Item
H2120348	Certificate of Analysis	Jun 09, 2025	P112689
F2415201	Certificate of Analysis	Mar 23, 2024	P112689
F2406201	Certificate of Analysis	Mar 20, 2024	P112689
F2406202	Certificate of Analysis	Mar 20, 2024	P112689
K1926176	Certificate of Analysis	Sep 08, 2023	P112689
C2322543	Certificate of Analysis	Feb 25, 2023	P112689
C2322540	Certificate of Analysis	Feb 25, 2023	P112689
C2322536	Certificate of Analysis	Feb 25, 2023	P112689
C2322537	Certificate of Analysis	Feb 25, 2023	P112689
C2322538	Certificate of Analysis	Feb 25, 2023	P112689
A2515107	Certificate of Analysis	Feb 25, 2023	P112689
C2322539	Certificate of Analysis	Feb 25, 2023	P112689

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Chemical and Physical Properties

Solubility	Solubility in water: Completely soluble; Very soluble in Benzene,Alcohol,Chloroform,Ether
Flash Point(°F)	320°F
Flash Point(°C)	160℃
Boil Point(°C)	272-274°C
Melt Point(°C)	67-68°C
Molecular Weight	138.160 g/mol
XLogP3	0.400
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	138.068 Da
Monoisotopic Mass	138.068 Da
Topological Polar Surface Area	40.500 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	87.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
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

How to Cite Aladdin Scientific Products?

1. Kunpeng Li,Rongzhen Zhang,Yan Xu,Zhimeng Wu,Jing Li,Xiaotian Zhou,Jiawei Jiang,Haiyan Liu,Rong Xiao. (2017-06-10) Sortase A-mediated crosslinked short-chain dehydrogenases/reductases as novel biocatalysts with improved thermostability and catalytic efficiency.. Scientific reports, 7 ((1)): (3081-3081).
2. Ping Wei, Ze-Wang Guo, Xiao-Ling Wu, Shan Liang, Xiao-Yang Ou, Pei Xu, Min-Hua Zong, Ji-Guo Yang, Wen-Yong Lou. (2019) Significantly enhancing the biocatalytic synthesis of chiral alcohols by semi-rationally engineering an anti-Prelog carbonyl reductase from Acetobacter sp. CCTCC M209061. Molecular Catalysis, 479 (110613).
3. Shaoyuan Guo, Xinli Tong, Jipeng Wang, Hang Tang. (2024) Selective aerobic oxidative C–C bond cleavage using a high-entropy oxide-derived multimetallic catalyst. Reaction Chemistry & Engineering,

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