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252794

Methyl 3-hydroxybenzoate

Name: Methyl 3-hydroxybenzoate
Brand: ALDRICH

99%

Synonym(s):

3-(Methoxycarbonyl)phenol, 3-Carbomethoxyphenol, 3-Hydroxybenzoic acid methyl ester, Methyl m-hydroxybenzoate, m-Carbomethoxyphenol, m-Hydroxybenzoic acid methyl ester

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About This Item

Linear Formula:

HOC₆H₄CO₂CH₃

CAS Number:

19438-10-9

Molecular Weight:

152.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24855238

EC Number:

243-071-5

Beilstein/REAXYS Number:

2208129

MDL number:

MFCD00002295

Assay:

99%

Form:

solid

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Properties

Quality Level

100

assay

99%

form

solid

bp

280-281 °C/709 mmHg (lit.)

mp

70-72 °C (lit.)

functional group

ester

SMILES string

COC(=O)c1cccc(O)c1

InChI

1S/C8H8O3/c1-11-8(10)6-3-2-4-7(9)5-6/h2-5,9H,1H3

InChI key

YKUCHDXIBAQWSF-UHFFFAOYSA-N

Description

Application

Methyl 3-hydroxybenzoate has been used in synthesis of:

3-hydroxybenzene-1,2-dicarbaldehyde
O-methyl O-[3-methyl-4-(methylthio)phenyl]O-(3-methylcarboxyphenyl) phosphorothioate

pictograms

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Investigation of the effect of hapten heterology on immunoassay sensitivity and development of an enzyme-linked immunosorbent assay for the organophosphorus insecticide fenthion.

Kim YJ, et al.

Analytica Chimica Acta, 94(1, 29-40 (2003)

Structural elucidation and synthesis of 3-hydroxybenzene-1,2-dicarbaldehyde from astigmatid mites.

T Sakata et al.

Bioscience, biotechnology, and biochemistry, 65(10), 2315-2317 (2002-01-05)

The structure of a novel aromatic compound contained in the unidentified Rhizoglyhus mite (Acaridae: Astigmata) was elucidated, without its isolation, to be 3-hydroxybenzene-1,2-dicarbaldehyde (tentatively named gamma-acaridial) by a combination of GC/MS and GC/FT-IR together with knowledge of related mite compounds.

Synthesis and Comparative Structure-Activity Study of Carbohydrate-Based Phenolic Compounds as α-Glucosidase Inhibitors and Antioxidants.

Shota Machida et al.

Molecules (Basel, Switzerland), 24(23) (2019-12-01)

Twenty-one natural and unnatural phenolic compounds containing a carbohydrate moiety were synthesized and their structure-activity relationship (SAR) was evaluated for α-glucosidase inhibition and antioxidative activity. Varying the position of the galloyl unit on the 1,5-anhydro-d-glucitol (1,5-AG) core resulted in changes

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Global Trade Item Number

SKU	GTIN
252794-100G	04061825973623
252794-25G	04061831810264