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Merck
CN

M13203

3-Methoxycatechol

99%

Synonym(s):

1,2-Dihydroxy-3-methoxybenzene, 3-Methoxypyrocatechol, Pyrogallol monomethyl ether

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About This Item

Linear Formula:
CH3OC6H3(OH)2
CAS Number:
934-00-9
Molecular Weight:
140.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24896634
EC Number:
213-276-4
Beilstein/REAXYS Number:
1909165
MDL number:
MFCD00002191

Key Documents

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Product Name

3-Methoxycatechol, 99%

InChI key

LPYUENQFPVNPHY-UHFFFAOYSA-N

InChI

1S/C7H8O3/c1-10-6-4-2-3-5(8)7(6)9/h2-4,8-9H,1H3

SMILES string

COc1cccc(O)c1O

assay

99%

bp

146-147 °C/15 mmHg (lit.)

mp

38-43 °C (lit.)

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5094
STBL2229
STBK6288
STBH0704
STBF8545V

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M Hirose et al.
Japanese journal of cancer research : Gann, 81(9), 857-861 (1990-09-01)
The effects of sodium nitrite (NaNO2) and catechol or 3-methoxycatechol in combination were examined in male F344 rats. Animals were treated with 0.3% NaNO2 in the drinking water and 0.8% catechol or 2% 3-methoxycatechol in powdered diet for 24 weeks.
M Kawabe et al.
Japanese journal of cancer research : Gann, 85(1), 17-25 (1994-01-01)
The effects of combined treatment with NaNO2 and phenolic compounds on N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) stomach carcinogenesis were investigated in F344 rats. In the first experiment, groups of 15-20 male rats were treated with an intragastric dose of 150 mg/kg body weight
Keith M Anderson et al.
The Journal of organic chemistry, 72(26), 9875-9880 (2007-11-30)
A novel universal support for deoxyribo- and ribonucleic acid synthesis has been developed. The support, constructed from 1,4-dimethoxycatechol, represents an improvement over existing universal supports because of its ability to cleave and deprotect under mild conditions in standard reagents. Because
Huayun Deng et al.
Pharmaceuticals (Basel, Switzerland), 6(4), 500-509 (2013-11-28)
Nearly 1% of all clinically used drugs are catecholics, a family of catechol-containing compounds. Using label-free dynamic mass redistribution and Tango β-arrestin translocation assays, we show that several catecholics, including benserazide, catechol, 3-methoxycatechol, pyrogallol, (+)-taxifolin and fenoldopam, display agonistic activity
M Hirose et al.
Cancer research, 53(1), 32-37 (1993-01-01)
Effects of simultaneous treatment with NaNO2 and butylated hydroxyanisole, catechol, or 3-methoxycatechol were examined in a rat multiorgan carcinogenesis model. Groups of 15 animals were given a single i.p. injection of 100 mg/kg of body weight diethylnitrosamine, 4 i.p. injections
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