methyl 3-hydroxybenzoate

benzoic acid, 3-hydroxy-, methyl ester

CAS: 19438-10-9 C8 H8 O3 MW: 152.14936000

All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers Found in Nature IUPAC Names M.W Index

Identification

Name	methyl 3-hydroxybenzoate
CAS Number	19438-10-9
EINECS	243-071-5
FDA UNII	569M9G3STJ
Molecular Formula	C8 H8 O3
Molecular Weight	152.14936000
MDL Number	MFCD00002295
Nikkaji Number	J47.816D
Beilstein	2208129
XlogP3	1.90 (est)

Regulatory

Physical Properties

Assay	95.00 to 100.00
Food Chemicals Codex Listed	No
Melting Point	73.00 °C. @ 760.00 mm Hg
Boiling Point	281.00 °C. @ 760.00 mm Hg, 283.00 to 284.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure	0.002000 mmHg @ 25.00 °C. (est)
Flash Point	260.00 °F. TCC ( 126.70 °C. ) (est)
logP (o/w)	1.890
Soluble in	alcohol
Insoluble in	water

No sensory data available

Safety Information

Preferred SDS	View
Oral/Parenteral Toxicity	Not determined
Dermal Toxicity	Not determined
Inhalation Toxicity	Not determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Category	natural substances and extractives
Recommendation for methyl 3-hydroxybenzoate usage levels up to	not for fragrance use.
Recommendation for methyl 3-hydroxybenzoate flavor usage levels up to	not for flavor use.

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19438-10-9 Methyl 3-hydroxybenzoate

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H0215 Methyl 3-hydroxybenzoate >98.0%(GC)(T)

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Potential Uses

None Found

Natural Occurrence

cichorium intybus root extract @ 0.64% Data orchis mascula securidaca longepedunculata

Synonyms

benzoic acid, 3-hydroxy-, methyl ester benzoic acid, m-hydroxy-, methyl ester m- carbomethoxyphenol meta- carbomethoxyphenol 3- hydroxybenzoic acid methyl ester m- hydroxybenzoic acid methyl ester meta- hydroxybenzoic acid methyl ester 3-( methoxycarbonyl)phenol methyl m-hydroxybenzoate methyl m-oxybenzoate methyl meta-hydroxybenzoate methyl meta-oxybenzoate PubMed: Purification and characterization of PrbA, a new esterase from Enterobacter cloacae hydrolyzing the esters of 4-hydroxybenzoic acid (parabens). PubMed: Structural elucidation and synthesis of 3-hydroxybenzene-1,2-dicarbaldehyde from astigmatid mites.