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328383

Sigma-Aldrich

mono-Methyl terephthalate

97%

Synonym(s):

4-(Carbomethoxy)benzoic acid, Hydrogen methyl terephthalate, Methyl 4-carboxybenzoate, Methyl p-phthalate, p-(Methoxycarbonyl)benzoic acid, p-Carbomethoxybenzoic acid

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About This Item

Linear Formula:
4-(HO2C)C6H4CO2CH3
CAS Number:
1679-64-7
Molecular Weight:
180.16
Beilstein:
1911082
EC Number:
216-849-7
MDL number:
MFCD00002557
UNSPSC Code:
12352100
PubChem Substance ID:
24859733
NACRES:
NA.22

Assay

97%

mp

220-223 °C (lit.)

SMILES string

COC(=O)c1ccc(cc1)C(O)=O

InChI

1S/C9H8O4/c1-13-9(12)7-4-2-6(3-5-7)8(10)11/h2-5H,1H3,(H,10,11)

InChI key

REIDAMBAPLIATC-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The inhibitory effect of new hydroxamic acid derivatives on melanogenesis.
Baek HS, et al.
ChemInform, 39(23) (2008)
A E Cury et al.
Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology, 24(2), 161-164 (1986-04-01)
Some of the lipids described in many fungi were found in Madurella grisea, in addition to other diethyl ether-soluble components with peculiar characteristics. One fraction structurally related to ethane diol (ethylene glycol) accounted for about 41% and a compound identified
Li J, et al.
International Biodeterioration & Biodegradation, 55(3), 223-232 (2005)

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