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Merck
CN

36684

3-Aminophenol

PESTANAL®, analytical standard

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About This Item

Linear Formula:
H2NC6H4OH
CAS Number:
591-27-5
Molecular Weight:
109.13
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755450
EC Number:
209-711-2
Beilstein/REAXYS Number:
636059
MDL number:
MFCD00007786

Key Documents

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Product Name

3-Aminophenol, PESTANAL®, analytical standard

InChI key

CWLKGDAVCFYWJK-UHFFFAOYSA-N

InChI

1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2

SMILES string

Nc1cccc(O)c1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

164 °C/11 mmHg (lit.)

mp

120-124 °C (lit.)

application(s)

agriculture
environmental

format

neat

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH6730
BCBW5080

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E Vasbinder et al.
Biomedical chromatography : BMC, 18(1), 55-63 (2004-02-12)
An ion-pair high performance liquid chromatographic method was developed for the simultaneous determination of p-aminosalicylic acid (PAS) and its degradation product m-aminophenol (MAP) in a newly developed multiparticular drug delivery system. Owing to the concentration differences of PAS and MAP
Jennifer A Reese et al.
Journal of the American Chemical Society, 126(36), 11387-11392 (2004-09-10)
Rotationally resolved electronic spectroscopy in the gas phase, in the absence and presence of an applied electric field, has been used to distinguish the two conformers of 3-aminophenol (3AP) on the basis of differences in their electric dipole moments. cis-3AP
O I Malykhina et al.
Sudebno-meditsinskaia ekspertiza, 49(1), 25-27 (2006-03-03)
The article presents the results of nitrobenzene and 3-aminohydroxibensene extraction from aqueous solutions by means of five organic solvents. The following factors influence on the extraction degree is shown: the nature of the extracting agent, aqueous phase pH, saturation of
Suresh Chandra Rastogi et al.
Contact dermatitis, 55(2), 95-100 (2006-08-26)
Contact allergy to hair dye ingredients, especially precursors and couplers, is a well-known entity among consumers having hair colouring done at home or at a hairdresser. The aim of the present investigation was to estimate consumer exposure to some selected
Hsiao-Shu Lee et al.
The Annals of occupational hygiene, 53(3), 289-296 (2009-03-13)
Skin irritation and contact allergies are skin disorders common to hairdressers. The predominant oxidative hair dye components, such as p-phenylenediamine (PPD) and aminophenol isomers, can cause contact dermatitis. Use of protective gloves can prevent dermal contact with skin irritants. This
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