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3-Aminophenol - ≥98%, high purity , CAS No.591-27-5

  • ≥98%
Item Number
A108481
Grouped product items
SKUSizeAvailabilityPrice Qty
A108481-25g
25g
In stock
$21.90
A108481-100g
100g
In stock
$36.90
A108481-250g
250g
In stock
$73.90
A108481-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$133.90
View related series
Oxygenated compounds phenol

Basic Description

Synonyms3-Aminophenol|591-27-5|M-AMINOPHENOL|3-Hydroxyaniline|m-Hydroxyaniline|Phenol, 3-amino-|3-Amino-1-hydroxybenzene|m-Hydroxyaminobenzene|Fouramine EG|Futramine EG|1-Amino-3-hydroxybenzene|Fourrine EG|3-amino-phenol|Pelagol EG|Tertral EG|Furro EG|Renal EG|Ur
Specifications & Purity≥98%
Storage TempProtected from light,Argon charged
Shipped InNormal
Product Description

3-Aminophenol has been used in the synthesis of disulfonated bis[4-(3-aminophenoxy)phenyl]sulfone (S-BAPS).
It can be used to synthesize:
Methyl 2-oxo-7-[(triphenylphosphoranylidene)amino]-2H-chromene-4-carboxylate by reacting with dimethyl acetylenedicarboxylate (DMAD) in the presence of triphenylphosphine.
3-Amino-2-cyclohexen-1-one via palladium-catalyzed hydrogenation.

Associated Targets

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RUNX1 Tbio Runt-related transcription factor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TXNRD1 Tclin Thioredoxin reductase 1, cytoplasmic 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NR1H4 Tclin Bile acid receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA14 Tclin Carbonic anhydrase 14 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA7 Tclin Carbonic anhydrase 7 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GLS Tchem Glutaminase kidney isoform, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488181383
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181383
IUPAC Name 3-aminophenol
INCHI InChI=1S/C6H7NO/c7-5-2-1-3-6(8)4-5/h1-4,8H,7H2
InChi Key CWLKGDAVCFYWJK-UHFFFAOYSA-N
Canonical SMILES C1=CC(=CC(=C1)O)N
Isomeric SMILES C1=CC(=CC(=C1)O)N
WGK Germany 2
RTECS SJ4900000
PubChem CID 11568
UN Number 2512
Packing Group III
Molecular Weight 109.13
Beilstein 636059
Reaxy-Rn 636059

Certificates

Certificate of Analysis(COA)

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15 results found

Lot NumberCertificate TypeDateItem
E2409335Certificate of AnalysisMay 22, 2024 A108481
E2409336Certificate of AnalysisMay 22, 2024 A108481
E2409337Certificate of AnalysisMay 22, 2024 A108481
B2207069Certificate of AnalysisNov 03, 2023 A108481
B2207070Certificate of AnalysisNov 03, 2023 A108481
B2207135Certificate of AnalysisNov 03, 2023 A108481
B2207136Certificate of AnalysisNov 03, 2023 A108481
E2127044Certificate of AnalysisMar 09, 2023 A108481
E2127066Certificate of AnalysisMar 09, 2023 A108481
E2127073Certificate of AnalysisMar 09, 2023 A108481
B2307198Certificate of AnalysisFeb 20, 2023 A108481
F1905037Certificate of AnalysisJan 05, 2023 A108481
G2021057Certificate of AnalysisMay 07, 2022 A108481
G2021056Certificate of AnalysisMay 07, 2022 A108481
K2329237Certificate of AnalysisDec 17, 2021 A108481

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Chemical and Physical Properties

SolubilitySoluble in water (35 mg/ml at 20°C), ether, alcohol, amyl alcohol, and benzene (slightly).
Sensitivityair sensitive ;light sensitive
Flash Point(°C)155℃
Boil Point(°C)164 °C/11 mmHg
Melt Point(°C)123℃

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS07
Signal Warning
Hazard Statements

H411:Toxic to aquatic life with long lasting effects

H302:Harmful if swallowed

H332:Harmful if inhaled

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P273:Avoid release to the environment.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P391:Collect spillage.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

P317:Get emergency medical help.

WGK Germany 2
RTECS SJ4900000
Reaxy-Rn 636059
Class 6.1
Merck Index 460

Related Documents

References

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Solution Calculators