p-Aminophenol - ≥98% , CAS No.123-30-8

Name: p-Aminophenol - ≥98% , CAS No.123-30-8
SKU: A110564
Availability: InStock

CAS: 123-30-8 Cat. No.: A110564 Formula: C₆H₇NO Molecular Weight: 109.13 Beilstein Registry Number: 385836 EC Number: 204-616-2

142 Citations COA

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p-Aminophenol - ≥98% CAS No(123-30-8) A110564 by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY ≥98%

Synonyms

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice,FedEx DG Service

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews

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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged Ships Wet ice,FedEx DG Service Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 142 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

4-Aminophenol (4-Hydroxyaniline) is an organic building block. Its quantification in water samples upto the detection limit of 8×10-10mol l-1 has been proposed by employing single-wall carbon nanotubes (SWNT)-nafion film coated glassy carbon electrodes. It is present as the main contaminant in pharmaceutical formulations of paracetamol. High-performance liquid chromatographic (HPLC) method with amperometric detection has been reported for its determination in various analgesic formulations. It has been reported to be formed from the reduction of 4-nitrophenol (Nip) under metal-free conditions catalyzed by N-doped graphene (NG).

Specifications

Synonyms

Specifications & Purity

≥98%

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice,FedEx DG Service

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

Pubchem Sid

508813260

Canonical Smiles

C1=CC(=CC=C1N)O

IUPAC Name

4-aminophenol

InChIKey

PLIKAWJENQZMHA-UHFFFAOYSA-N

INCHI

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

Isomeric SMILES

C1=CC(=CC=C1N)O

WGK Germany

RTECS

SJ5075000

UN Number

2512

Packing Group

III

Molecular Weight

109.13

Beilstein

385836

Reaxy-Rn

385836

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=385836&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Aniline and substituted anilines

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Aniline and substituted anilines
Intermediate Tree Nodes	Not available
Direct Parent	Aniline and substituted anilines
Alternative Parents	p-Aminophenols 1-hydroxy-2-unsubstituted benzenoids Primary amines Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	P-aminophenol - Aniline or substituted anilines - Aminophenol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors	a phenol
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D Structure

Associated Targets(Human)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

VDR Tclin Vitamin D receptor (26531 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)

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CA3 Tclin Carbonic anhydrase III (753 Activities)

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CA6 Tclin Carbonic anhydrase VI (993 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

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GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)

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CA5B Tclin Carbonic anhydrase VB (957 Activities)

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CA5A Tclin Carbonic anhydrase VA (1168 Activities)

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CA14 Tclin Carbonic anhydrase XIV (1305 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)

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NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)

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CASP1 Tchem Caspase-1 (6235 Activities)

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ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

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CA12 Tclin Carbonic anhydrase XII (6231 Activities)

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UGT1A4 Tbio UDP-glucuronosyltransferase 1A4 (288 Activities)

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CA9 Tclin Carbonic anhydrase IX (8255 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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HL-60 (67320 Activities)

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MIA PaCa-2 (5949 Activities)

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HepG2 (196354 Activities)

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Lymphoblastoid cell (5959 Activities)

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FEN1 Tchem Flap endonuclease 1 (12055 Activities)

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HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT2B7 Tchem UDP-glucuronosyltransferase 2B7 (787 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT2B17 Tbio UDP-glucuronosyltransferase 2B17 (197 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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EP300 Tchem Histone acetyltransferase p300 (1259 Activities)

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KAT2B Tchem Histone acetyltransferase PCAF (884 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLK Tbio DNA polymerase kappa (8653 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLI Tchem DNA polymerase iota (116820 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)

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EYA2 Tbio Eyes absent homolog 2 (5884 Activities)

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APOBEC3G Tchem DNA dC->dU-editing enzyme APOBEC-3G (12481 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)

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KAT8 Tchem Histone acetyltransferase KAT8 (178 Activities)

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RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)

Discover Target: RUNX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Ca7 Carbonic anhydrase VII (3 Activities)

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Cruzipain (33337 Activities)

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Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Ca13 Carbonic anhydrase XIII (322 Activities)

Discover Target: Ca13

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA4 Carbonic anhydrase IV (1713 Activities)

Discover Target: CA4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Faah Anandamide amidohydrolase (3907 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Bacillus subtilis (32866 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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dnaB Replicative DNA helicase (15 Activities)

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lef Anthrax lethal factor (7585 Activities)

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Luciferin 4-monooxygenase (66902 Activities)

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Ca15 Carbonic anhydrase 15 (173 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

recA Protein RecA (2211 Activities)

Discover Target: recA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

62 results found

Lot Number	Certificate Type	Date	Item
J2330099	Certificate of Analysis	Sep 01, 2026	A110564
H2302031	Certificate of Analysis	Sep 01, 2026	A110564
I2614222	Certificate of Analysis	Aug 29, 2026	A110564
I2614223	Certificate of Analysis	Aug 29, 2026	A110564
I2614224	Certificate of Analysis	Aug 29, 2026	A110564
I2614225	Certificate of Analysis	Aug 29, 2026	A110564
I2614226	Certificate of Analysis	Aug 29, 2026	A110564
K2520273	Certificate of Analysis	Aug 04, 2026	A110564
K2520261	Certificate of Analysis	Aug 04, 2026	A110564
K2520271	Certificate of Analysis	Aug 04, 2026	A110564
J2431074	Certificate of Analysis	Aug 03, 2026	A110564
J2431117	Certificate of Analysis	Aug 03, 2026	A110564
D2424084	Certificate of Analysis	Aug 03, 2026	A110564
E2614222	Certificate of Analysis	Apr 30, 2026	A110564
E2614220	Certificate of Analysis	Apr 30, 2026	A110564
E2614224	Certificate of Analysis	Apr 30, 2026	A110564
E2614223	Certificate of Analysis	Apr 30, 2026	A110564
E2614221	Certificate of Analysis	Apr 30, 2026	A110564
K2520263	Certificate of Analysis	Oct 29, 2025	A110564
K2520262	Certificate of Analysis	Oct 29, 2025	A110564
E2527159	Certificate of Analysis	Jun 05, 2025	A110564
F2520177	Certificate of Analysis	May 26, 2025	A110564
F2520178	Certificate of Analysis	May 26, 2025	A110564
F2520233	Certificate of Analysis	May 26, 2025	A110564
F2520106	Certificate of Analysis	May 26, 2025	A110564
J2509121	Certificate of Analysis	May 26, 2025	A110564
K2427118	Certificate of Analysis	Nov 14, 2024	A110564
K2427119	Certificate of Analysis	Nov 14, 2024	A110564
K2427141	Certificate of Analysis	Nov 14, 2024	A110564
K2427120	Certificate of Analysis	Nov 14, 2024	A110564
K2427235	Certificate of Analysis	Nov 14, 2024	A110564
J2415700	Certificate of Analysis	Sep 27, 2024	A110564
J2415742	Certificate of Analysis	Sep 27, 2024	A110564
J2415743	Certificate of Analysis	Sep 27, 2024	A110564
J2415763	Certificate of Analysis	Sep 27, 2024	A110564
J2431286	Certificate of Analysis	Jul 27, 2024	A110564
J2431285	Certificate of Analysis	Jul 27, 2024	A110564
J2431276	Certificate of Analysis	Jul 27, 2024	A110564
J2431038	Certificate of Analysis	Jul 27, 2024	A110564
J2430074	Certificate of Analysis	Jul 27, 2024	A110564
G2418378	Certificate of Analysis	Apr 29, 2024	A110564
G2416556	Certificate of Analysis	Apr 29, 2024	A110564
H2406169	Certificate of Analysis	Apr 29, 2024	A110564
B2512085	Certificate of Analysis	Apr 29, 2024	A110564
H2406167	Certificate of Analysis	Apr 29, 2024	A110564
H2406168	Certificate of Analysis	Apr 29, 2024	A110564
H2405061	Certificate of Analysis	Apr 11, 2024	A110564
D2424114	Certificate of Analysis	Apr 11, 2024	A110564
D2424087	Certificate of Analysis	Apr 11, 2024	A110564
J2330129	Certificate of Analysis	Oct 20, 2023	A110564
J2330098	Certificate of Analysis	Oct 20, 2023	A110564
H2302029	Certificate of Analysis	Jul 11, 2023	A110564
H2302030	Certificate of Analysis	Jul 11, 2023	A110564
H2302032	Certificate of Analysis	Jul 11, 2023	A110564
B2308198	Certificate of Analysis	Jan 04, 2023	A110564
B2308200	Certificate of Analysis	Jan 04, 2023	A110564
B2308196	Certificate of Analysis	Jan 04, 2023	A110564
I2207257	Certificate of Analysis	Aug 23, 2022	A110564
I2207256	Certificate of Analysis	Aug 23, 2022	A110564
I2207252	Certificate of Analysis	Aug 23, 2022	A110564
I2207227	Certificate of Analysis	Aug 23, 2022	A110564
F2124049	Certificate of Analysis	Apr 26, 2022	A110564

Chemical and Physical Properties

Solubility	Soluble in acetonitrile, ethyl acetate, acetone, hot water, dimethylsulfoxide and alkalies. Slightly soluble in toluene, diethyl ether, ethanol, trifluoroacetic acid and cold water. Insoluble in benzene and chloroform.
Sensitivity	heat sensitive; light sensitive;air sensitive;Moisture sensitive
Flash Point(°C)	189℃
Boil Point(°C)	284°C
Melt Point(°C)	176-188°C
Molecular Weight	109.130 g/mol
XLogP3	0.000
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	109.053 Da
Monoisotopic Mass	109.053 Da
Topological Polar Surface Area	46.300 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	66.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Documents & Articles

Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines

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📚 Citations by Application

Polymer synthesis & polymerization40

Other applications45

Organic synthesis — reaction medium84

Cross-coupling reactions6

Extraction & workup solvent29

Chromatography (HPLC / GC / TLC)6

Electrochemistry & battery electrolyte40

Drug / compound screening26

Cell viability3

Cell proliferation1

Nanoparticle / material biocompatibility5

Industrial & non-pharma application12

Spectroscopy sample preparation11

Grignard & organometallic chemistry1

Cytotoxicity screening3

Cancer cell line characterization3

Controlled-release & nanoparticle carrier1

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p-Aminophenol - analytical standard, ≥99.5% , CAS No.123-30-8

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Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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