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D144002

Sigma-Aldrich

3-(Dimethylamino)phenol

97%

Sinónimos:

N,N-Dimethyl-3-aminophenol

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About This Item

Fórmula lineal:
(CH3)2NC6H4OH
Número de CAS:
99-07-0
Peso molecular:
137.18
Beilstein/REAXYS Number:
774631
EC Number:
202-727-0
MDL number:
MFCD00002264
UNSPSC Code:
12352100
PubChem Substance ID:
24893440
NACRES:
NA.22

assay

97%

form

crystals

mp

82-84 °C (lit.)

SMILES string

CN(C)c1cccc(O)c1

InChI

1S/C8H11NO/c1-9(2)7-4-3-5-8(10)6-7/h3-6,10H,1-2H3

InChI key

MESJRHHDBDCQTH-UHFFFAOYSA-N

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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_germany

WGK 3

flash_point_f

298.4 °F - closed cup

flash_point_c

148 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Anežka Tichá et al.
The Journal of biological chemistry, 292(7), 2703-2713 (2017-01-11)
Rhomboid proteases are increasingly being explored as potential drug targets, but their potent and specific inhibitors are not available, and strategies for inhibitor development are hampered by the lack of widely usable and easily modifiable
Bozena Bukowska et al.
Toxicology in vitro : an international journal published in association with BIBRA, 21(8), 1574-1580 (2007-07-17)
3-(Dimethylamino)phenol (3-DMAP) exists in the environment as a transformation product of ureic herbicides and may also be considered as a derivative of phenoxyherbicides. In this study, the activity of glutathione peroxidase, catalase and superoxide dismutase, as well as the level
Avi Weissberg et al.
Journal of chromatography. A, 1512, 71-77 (2017-07-18)
A methodology for sensitive determination of sarin (GB), soman (GD) and cyclosarin (GF) chemical warfare agents in aqueous media was developed. The method incorporates direct derivatization with 2-[(dimethylamino)methyl]phenol (2-DMAMP), a commercially available, water-soluble reagent, followed by LC-ESI-MS/MS analysis in the
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following

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