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3,5-Dihydroxybenzaldehyde - 98%, high purity , CAS No.26153-38-8

    Grade & Purity:
  • ≥98%
In stock
Item Number
D120469
Grouped product items
SKU Size
Availability
Price Qty
D120469-200mg
200mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$23.90
D120469-1g
1g
3
$84.90
D120469-5g
5g
2
$339.90
D120469-10g
10g
1
$543.90
View related series
Organic synthetic blocks (17)

Basic Description

Synonyms AM20120664 | AS-32854 | AKOS005258327 | 3,5-dihydroxy benzaldehyde | SCHEMBL37131 | BBL101356 | PD131130 | EINECS 247-479-4 | InChI=1/C7H6O3/c8-4-5-1-6(9)3-7(10)2-5/h1-4,9-10 | STL555152 | MFCD00016611 | W-107196 | Q27121981 | DTXSID60180776 | A20612 | .a
Specifications & Purity ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

3,5-Dihydroxybenzaldehyde is suitable for use in the synthesis of 3,5-dihydroxyphenylglycine (3,5-DHPG). It may be used in the synthesis of: fulgide7 3,5-bis(undeca-4,6-diynyloxy)benzaldehyde 3,5-didodecyloxybenzaldehyde 1′-methyl-1′,5′-dihydro-2′-(3,5-bis(undeca-4,6-diynyloxy)phenyl)-1H-pyrrolo[3′,4′:1,9](C60-Ih)[5,6]fullerene (F2D)

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbonyl compounds
Intermediate Tree Nodes Aldehydes - Aryl-aldehydes - Benzaldehydes
Direct Parent Hydroxybenzaldehydes
Alternative Parents Resorcinols  Benzoyl derivatives  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Hydroxybenzaldehyde - Resorcinol - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
External Descriptors dihydroxybenzaldehyde

Names and Identifiers

Pubchem Sid 504756215
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504756215
IUPAC Name 3,5-dihydroxybenzaldehyde
INCHI InChI=1S/C7H6O3/c8-4-5-1-6(9)3-7(10)2-5/h1-4,9-10H
InChIKey HAQLHRYUDBKTJG-UHFFFAOYSA-N
Smiles C1=C(C=C(C=C1O)O)C=O
Isomeric SMILES C1=C(C=C(C=C1O)O)C=O
WGK Germany 3
Molecular Weight 138.12
Beilstein 1930147
Reaxy-Rn 1930147
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1930147&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.

7 results found

Lot Number Certificate Type Date Item
C2405412 Certificate of Analysis Mar 11, 2024 D120469
B2522169 Certificate of Analysis Mar 11, 2024 D120469
C2405398 Certificate of Analysis Mar 11, 2024 D120469
C2405413 Certificate of Analysis Mar 11, 2024 D120469
E2417400 Certificate of Analysis Mar 02, 2024 D120469
H2229220 Certificate of Analysis Sep 01, 2022 D120469
H2229223 Certificate of Analysis Sep 01, 2022 D120469

Chemical and Physical Properties

Solubility Soluble in ethanol and diethyl ether.
Sensitivity Air Sensitive
Melt Point(°C) 158-161°C
Molecular Weight 138.120 g/mol
XLogP3 0.700
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Exact Mass 138.032 Da
Monoisotopic Mass 138.032 Da
Topological Polar Surface Area 57.500 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 114.000
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

1. Xuesong Gu, Shubo Xie, Qiang Chen, Shufeng Chen, Haiying Zhao, Zhanxi Bian.  (2018)  Anti-migration and burning rate catalytic performances of novel ferrocene-based porphyrins and their transition-metal complexes.  NEW JOURNAL OF CHEMISTRY,  42  (16): (13319-13328). 
2. Rongbin Huang, Lei Xiang, Ying Liu, Xiangping Deng, Xuan Cao, Lanfang Li, Cuiyun Yu, Yanming Chen, Guotao Tang.  (2016)  Synthesis and in vitro evaluation of pH-sensitive PEG-I-dC16 block polymer micelles for anticancer drug delivery.  JOURNAL OF PHARMACY AND PHARMACOLOGY,  68  (6): (751-761). 

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