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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/REAXYS Number:
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.)

functional group

carboxylic acid

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ1120
MKCK2536
MKBW6800V
MKBV0279V
03410DJ

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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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