missing translation for 'onlineSavingsMsg'
Learn More

Salicylaldehyde, 99%

CAS: 90-02-8 | C7H6O2 | 122.12 g/mol

$65.49 - $637.12

Chemical Identifiers

CAS 90-02-8
Molecular Formula C7H6O2
Molecular Weight (g/mol) 122.12
MDL Number MFCD00003317
InChI Key SMQUZDBALVYZAC-UHFFFAOYSA-N
Synonym salicylaldehyde, o-hydroxybenzaldehyde, o-formylphenol, salicylal, 2-formylphenol, benzaldehyde, 2-hydroxy, salicylic aldehyde, salicyladehyde, 2-hydroxy-benzaldehyde, benzaldehyde, o-hydroxy
PubChem CID 6998
ChEBI CHEBI:16008
IUPAC Name 2-hydroxybenzaldehyde
SMILES OC1=CC=CC=C1C=O
View More Specs

Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1383322
View Documents
Thermo Scientific Chemicals
A1383322
100 g
Each for $65.49
Only null left
 
AAA1383336
View Documents
Thermo Scientific Chemicals
A1383336
500 g
Each for $150.33
Only null left
 
AAA138330E
View Documents
Thermo Scientific Chemicals
A138330E
2500 g
Each for $637.12
Only null left
 
Description

Description

Precursor to a variety of chelating agents.Salicylaldehyde is used as a precursor to prepare catechol, benzofuran, salicylaldehydimine and 3-carbethoxycoumarin. It is used for colorimetric assay of isoleucine as well as utilized for the determination of primary amine by fluorescence method. It is a key starting material to a various chelating agents. It is used as flavor and fragrance components. Its derivative salicylaldehyde thiosemicarbazone is used for the simultaneous determination of molybdenum and iron by spectrophotometric method.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Precursor to a variety of chelating agents.Salicylaldehyde is used as a precursor to prepare catechol, benzofuran, salicylaldehydimine and 3-carbethoxycoumarin. It is used for colorimetric assay of isoleucine as well as utilized for the determination of primary amine by fluorescence method. It is a key starting material to a various chelating agents. It is used as flavor and fragrance components. Its derivative salicylaldehyde thiosemicarbazone is used for the simultaneous determination of molybdenum and iron by spectrophotometric method.

Solubility
Miscible with alcohol, ether, acetone, benzene and most organic solvents. Slightly miscible with water.

Notes
Incompatible with acids, strong reducing agents, strong oxidizing agents, strong bases and halogens.
Specifications

Chemical Identifiers

90-02-8
122.12
SMQUZDBALVYZAC-UHFFFAOYSA-N
6998
2-hydroxybenzaldehyde
C7H6O2
MFCD00003317
salicylaldehyde, o-hydroxybenzaldehyde, o-formylphenol, salicylal, 2-formylphenol, benzaldehyde, 2-hydroxy, salicylic aldehyde, salicyladehyde, 2-hydroxy-benzaldehyde, benzaldehyde, o-hydroxy
CHEBI:16008
OC1=CC=CC=C1C=O

Specifications

90-02-8
1.168
76°C (168°F)
C7H6O2
MFCD00003317
471388
14,8326
Miscible with alcohol,ether,acetone,benzene and most organic solvents. Slightly miscible with water.
OC1=CC=CC=C1C=O
122.12
CHEBI:16008
99%
Salicylaldehyde
°C to 7°C
197°C
99%
1.573
100 g
Air and light sensitive
salicylaldehyde, o-hydroxybenzaldehyde, o-formylphenol, salicylal, 2-formylphenol, benzaldehyde, 2-hydroxy, salicylic aldehyde, salicyladehyde, 2-hydroxy-benzaldehyde, benzaldehyde, o-hydroxy
SMQUZDBALVYZAC-UHFFFAOYSA-N
2-hydroxybenzaldehyde
6998
122.12
Liquid
Videos
Safety and Handling

Safety and Handling

GHS H Statement
H302-H315-H319-H335-H227

P210-P235-P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P309+P311-P312-P314-P330-P332+P313-P361-P363-P370+P378q-P501c

H227-H302-H311-H315-H319-H335

DOTInformation : Hazard Class: 6.1; Packaging Group: III

EINECSNumber : 201-961-0

RTECSNumber : VN5250000

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
missing translation for 'documents'

missing translation for 'documents'

RUO – Research Use Only