Skip to Content
Merck
CN

Key Documents

View All Documentation

03273

Salicylaldehyde

analytical standard

Synonym(s):

2-Hydroxybenzaldehyde

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
2-(HO)C6H4CHO
CAS Number:
90-02-8
Molecular Weight:
122.12
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329747580
MDL number:
MFCD00003317
Beilstein/REAXYS Number:
471388
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

grade

analytical standard

Quality Level

100

vapor density

4.2 (vs air)

vapor pressure

1 mmHg ( 33 °C)

assay

≥98.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.573

bp

197 °C (lit.)

mp

1-2 °C (lit.)

density

1.146 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

Oc1ccccc1C=O

InChI

1S/C7H6O2/c8-5-6-3-1-2-4-7(6)9/h1-5,9H

InChI key

SMQUZDBALVYZAC-UHFFFAOYSA-N

Still not finding the right product?

Explore all of our products under Salicylaldehyde

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN4125
BCCL0336
BCCG3424
BCCF0565
BCCD4695

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Stephen K Murphy et al.
Organic letters, 13(23), 6216-6219 (2011-11-09)
A method has been developed for the intermolecular hydroacylation of homoallyl alcohols with salicylaldehydes to furnish homoaldol products in 50-98% yields. The method also applies to the hydroacylation of 2-hydroxystyrenes. This work highlights the use of hydroacylation as a unified
Mirta Rubčić et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(18), 5620-5631 (2012-03-27)
The Schiff base derived from salicylaldehyde and 2-amino-3-hydroxypyridine affords a diversity of solid forms, two polymorphic pairs of the enol-imino (D1 a and D1 b) and keto-amino (D2 a and D2 b) desmotropes. The isolated phases, identified by IR spectroscopy, X-ray crystallography, and (13)C
Wen-Yong Han et al.
Organic letters, 14(4), 976-979 (2012-02-02)
The catalytic enantioselective three-component Petasis reaction among salicylaldehydes, amines, and organoboronic acids with a newly designed thiourea-binol catalyst is presented. A broad range of alkylaminophenols can be obtained in good yield (up to 92%) and good to high enantioselectivity (up
View All Related Papers

Global Trade Item Number

SKUGTIN
03273-5ML-F04061838618269
03273-1ML-F04061838185600