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3,4-Dihydroxybenzyl Alcohol - >96.0%, high purity , CAS No.3897-89-0

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3,4-Dihydroxybenzyl Alcohol - >96.0%, high purity , CAS No.3897-89-0

2 Citations

COA

Grade & Purity:

≥96%

Cas Number: 3897-89-0
Molecular Weight: 140.14
MDL number: MFCD00210409
PubChem CID: 100733
PubChem SID: 504756465

In stock

Item Number

D155345

Grouped product items
SKU	Size	Availability	Price
D155345-200mg	200mg	3	$28.90
D155345-1g	1g	2	$108.90
D155345-5g	5g	2	$329.90

View related series

Oxygenated compounds (806) phenol (506)

Basic Description

Synonyms	1,2-Benzenediol, 4-(hydroxymethyl)- \| EN300-1263448 \| 4-Hydroxymethylpyrocatechol \| Protocatechuic alcohol \| Adelheidsquelle \| UNII-61H4T033E5 \| BENZYL ALCOHOL, 3,4-DIHYDROXY- \| Q1765796 \| 1, 4-(hydroxymethyl)- \| 3,4-Dihydroxybenzyl alcohol \| A824358 \| 1-
Specifications & Purity	≥96%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Benzenediols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Benzenediols
Intermediate Tree Nodes	Not available
Direct Parent	Catechols
Alternative Parents	Benzyl alcohols 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Primary alcohols Hydrocarbon derivatives Aromatic alcohols
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Catechol - Benzyl alcohol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - 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 catechols. These are compounds containing a 1,2-benzenediol moiety.
External Descriptors	catechols
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)

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

NA Neuraminidase (1107 Activities)

Discover Target: NA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MDCK (10148 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	504756465
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756465
IUPAC Name	4-(hydroxymethyl)benzene-1,2-diol
INCHI	InChI=1S/C7H8O3/c8-4-5-1-2-6(9)7(10)3-5/h1-3,8-10H,4H2
InChIKey	PCYGLFXKCBFGPC-UHFFFAOYSA-N
Smiles	C1=CC(=C(C=C1CO)O)O
Isomeric SMILES	C1=CC(=C(C=C1CO)O)O
Molecular Weight	140.14
Reaxy-Rn	1862353
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1862353&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.

3 results found

Lot Number	Certificate Type	Date	Item
A2309703	Certificate of Analysis	Jul 06, 2022	D155345
A2309704	Certificate of Analysis	Jul 06, 2022	D155345
A2309702	Certificate of Analysis	Jul 06, 2022	D155345

Chemical and Physical Properties

Sensitivity	Air Sensitive,Heat Sensitive
Melt Point(°C)	117 °C
Molecular Weight	140.140 g/mol
XLogP3	0.100
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	140.047 Da
Monoisotopic Mass	140.047 Da
Topological Polar Surface Area	60.700 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	105.000
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

How to Cite Aladdin Scientific Products?

1. 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).
2. Wen-Kai Liu, Bing-Mei Su, Xin-Qi Xu, Lian Xu, Juan Lin. (2024) Multienzymatic Cascade for Synthesis of Hydroxytyrosol via Two-Stage Biocatalysis. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 72 (27): (15293-15300).

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