Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni

🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature,Argon charged Ships FedEx DG Service Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 1528 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

FedEx DG Service

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

488179585

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488179585

Sorrisi canonici

C1=CC=C(C=C1)O

IUPAC Name

phenol

InChIKey

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

INCHI

1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H

Isomeri SMILES

C1=CC=C(C=C1)O

WGK Germania

RTECS

SJ3325000

Numero UN

1671

Gruppo di imballaggio

Peso molecolare

94.11

Beilstein

969616

Reaxy-Rn

969616

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=969616&ln=

Documentazione

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Classe Phenols
    - Subclass 1-hydroxy-4-unsubstituted benzenoids

Kingdom	Organic compounds
Superclass	Benzenoids
Classe	Phenols
Subclass	1-hydroxy-4-unsubstituted benzenoids
Intermediate Tree Nodes	Not available
Direct Parent	1-hydroxy-4-unsubstituted benzenoids
Alternative Parents	1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Organooxygen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
Descrizione	This compound belongs to the class of organic compounds known as 1-hydroxy-4-unsubstituted benzenoids. These are phenols that are unsubstituted at the 4-position.
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

Struttura 3D

Obiettivi associati (umani)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

Discover Target: PDE5A

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

EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

Discover Target: EGFR

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

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

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

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

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

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

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

HMGCR Tclin HMG-CoA reductase (2475 Activities)

Discover Target: HMGCR

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

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

Discover Target: NR3C1

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

INSR Tclin Insulin receptor (5558 Activities)

Discover Target: INSR

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

PGR Tclin Progesterone receptor (8562 Activities)

Discover Target: PGR

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

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

Discover Target: ADRB2

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

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

Discover Target: CHRM2

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

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

Discover Target: ADRB1

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

HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

Discover Target: HTR1A

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

ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

Discover Target: ADRA2A

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

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

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

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

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

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

Discover Target: ACE

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

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

Discover Target: DRD2

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

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

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

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

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

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

Discover Target: CNR1

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

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

Discover Target: DRD1

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

DRD4 Tchem Dopamine D4 receptor (7907 Activities)

Discover Target: DRD4

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

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

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

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

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

Discover Target: SLC6A2

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

HRH2 Tclin Histamine H2 receptor (5428 Activities)

Discover Target: HRH2

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

ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

Discover Target: ADRA1D

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

HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

Discover Target: HTR1B

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

HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

Discover Target: HTR2A

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

HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

Discover Target: HTR2C

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

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

Discover Target: ADORA1

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

CALCR Tclin Calcitonin receptor (2215 Activities)

Discover Target: CALCR

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

SLC6A4 Tclin Serotonin transporter (12625 Activities)

Discover Target: SLC6A4

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

ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

Discover Target: ADRA1A

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

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

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

HRH1 Tclin Histamine H1 receptor (7573 Activities)

Discover Target: HRH1

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

ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

Discover Target: ADRA1B

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

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

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

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

Discover Target: DRD3

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

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

Discover Target: PPARG

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

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

Discover Target: AVPR1A

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

OPRD1 Tclin Delta opioid receptor (15096 Activities)

Discover Target: OPRD1

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

OPRK1 Tclin Kappa opioid receptor (16155 Activities)

Discover Target: OPRK1

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

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

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

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

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

HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

Discover Target: HTR4

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

PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

Discover Target: PDE3A

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

ESR2 Tclin Estrogen receptor beta (9272 Activities)

Discover Target: ESR2

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

CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

Discover Target: CYSLTR1

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

Obiettivi associati (non umani)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

Discover Target: Agtr2

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

Mc4r Melanocortin receptor 4 (1205 Activities)

Discover Target: Mc4r

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

Sult1a1 Aryl sulfotransferase (136 Activities)

Discover Target: Sult1a1

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

Ca7 Carbonic anhydrase VII (3 Activities)

Discover Target: Ca7

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

Ltc4s Leukotriene C4 synthase (1 Activities)

Discover Target: Ltc4s

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

Sigmar1 Sigma opioid receptor (160 Activities)

Discover Target: Sigmar1

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

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

Discover Target: Npy1r

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

Cckar Cholecystokinin A receptor (90 Activities)

Discover Target: Cckar

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

Nos2 Nitric oxide synthase, inducible (3573 Activities)

Discover Target: Nos2

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

Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

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

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

Mmp9 Matrix metalloproteinase 9 (38 Activities)

Discover Target: Mmp9

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

Carbonic anhydrase (69 Activities)

Explore this target

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

Staphylococcus aureus (210822 Activities)

Explore this target

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

Aspergillus niger (16508 Activities)

Explore this target

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

Bacillus subtilis (32866 Activities)

Explore this target

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

Plasmodium falciparum (966862 Activities)

Explore this target

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

Lithobates pipiens (29 Activities)

Explore this target

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

Xenopus laevis (337 Activities)

Explore this target

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

Mus musculus (284745 Activities)

Explore this target

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

CHO (4503 Activities)

Explore this target

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

L1210 (27553 Activities)

Explore this target

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

E Lysozyme (95 Activities)

Discover Target: E

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

norA Quinolone resistance protein norA (2171 Activities)

Discover Target: norA

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Ca15 Carbonic anhydrase 15 (173 Activities)

Discover Target: Ca15

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

mtcA1 Uncharacterized protein Rv1284/MT1322 (182 Activities)

Discover Target: mtcA1

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

PROBABLE TRANSMEMBRANE CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) (107 Activities)

Explore this target

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

Colon (26 Activities)

Explore this target

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)

Discover Target: Nfe2l2

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

CAN2 Carbonic anhydrase 2 (140 Activities)

Discover Target: CAN2

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

Gabrg2 GABA-A receptor; alpha-1/beta-2/gamma-2 (554 Activities)

Discover Target: Gabrg2

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

Glra2 Glycine receptor (1745 Activities)

Discover Target: Glra2

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

SARS-CoV-2 (38078 Activities)

Explore this target

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

Meccanismi d'azione

Certificati (CoA, COO, BSE/TSE e tabella di analisi)

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.

114 results found

Lot Number	Certificate Type	Data	Oggetto
H2627824	Certificate of Analysis	Sep 05, 2026	P128316
H2627825	Certificate of Analysis	Sep 05, 2026	P128316
H2627826	Certificate of Analysis	Sep 05, 2026	P128316
F2625266	Certificate of Analysis	Jul 01, 2026	P128316
F2625267	Certificate of Analysis	Jul 01, 2026	P128316
F2625296	Certificate of Analysis	Jul 01, 2026	P128316
F2610216	Certificate of Analysis	Jun 22, 2026	P128316
F2610217	Certificate of Analysis	Jun 22, 2026	P128316
F2610230	Certificate of Analysis	Jun 22, 2026	P128316
C2631349	Certificate of Analysis	Apr 07, 2026	P128316
C2631350	Certificate of Analysis	Apr 07, 2026	P128316
C2631351	Certificate of Analysis	Apr 07, 2026	P128316
D2616147	Certificate of Analysis	Apr 07, 2026	P128316
D2616148	Certificate of Analysis	Apr 07, 2026	P128316
D2616152	Certificate of Analysis	Apr 07, 2026	P128316
C2604219	Certificate of Analysis	Mar 12, 2026	P128316
A2630540	Certificate of Analysis	Feb 05, 2026	P128316
A2630541	Certificate of Analysis	Feb 05, 2026	P128316
L2512576	Certificate of Analysis	Dec 27, 2025	P128316
L2512577	Certificate of Analysis	Dec 27, 2025	P128316
L2512194	Certificate of Analysis	Dec 23, 2025	P128316
L2512195	Certificate of Analysis	Dec 23, 2025	P128316
L2512196	Certificate of Analysis	Dec 23, 2025	P128316
L2505609	Certificate of Analysis	Dec 12, 2025	P128316
L2505610	Certificate of Analysis	Dec 12, 2025	P128316
L2505611	Certificate of Analysis	Dec 12, 2025	P128316
K2506585	Certificate of Analysis	Nov 12, 2025	P128316
K2506589	Certificate of Analysis	Nov 12, 2025	P128316
K2506586	Certificate of Analysis	Nov 12, 2025	P128316
K2506590	Certificate of Analysis	Nov 12, 2025	P128316
J2524727	Certificate of Analysis	Nov 04, 2025	P128316
J2524728	Certificate of Analysis	Nov 04, 2025	P128316
J2524738	Certificate of Analysis	Nov 04, 2025	P128316
J2524730	Certificate of Analysis	Nov 04, 2025	P128316
I2515301	Certificate of Analysis	Sep 28, 2025	P128316
I2515302	Certificate of Analysis	Sep 28, 2025	P128316
I2515303	Certificate of Analysis	Sep 28, 2025	P128316
H2507024	Certificate of Analysis	Aug 13, 2025	P128316
H2507025	Certificate of Analysis	Aug 13, 2025	P128316
H2507026	Certificate of Analysis	Aug 13, 2025	P128316
E2526466	Certificate of Analysis	Jun 05, 2025	P128316
E2526467	Certificate of Analysis	Jun 05, 2025	P128316
B2525079	Certificate of Analysis	Mar 05, 2025	P128316
B2525083	Certificate of Analysis	Mar 05, 2025	P128316
B2525075	Certificate of Analysis	Mar 05, 2025	P128316
A2515228	Certificate of Analysis	Feb 22, 2025	P128316
A2515229	Certificate of Analysis	Feb 21, 2025	P128316
A2515232	Certificate of Analysis	Feb 21, 2025	P128316
L2410384	Certificate of Analysis	Dec 16, 2024	P128316
L2410386	Certificate of Analysis	Dec 16, 2024	P128316
L2410233	Certificate of Analysis	Dec 16, 2024	P128316
J2425321	Certificate of Analysis	Oct 31, 2024	P128316
J2425322	Certificate of Analysis	Oct 31, 2024	P128316
J2425326	Certificate of Analysis	Oct 31, 2024	P128316
I2420124	Certificate of Analysis	Sep 27, 2024	P128316
I2420314	Certificate of Analysis	Sep 27, 2024	P128316
I2420315	Certificate of Analysis	Sep 27, 2024	P128316
I2403152	Certificate of Analysis	Sep 10, 2024	P128316
I2403164	Certificate of Analysis	Sep 10, 2024	P128316
I2403165	Certificate of Analysis	Sep 09, 2024	P128316
G2419517	Certificate of Analysis	Aug 05, 2024	P128316
I2424009	Certificate of Analysis	Aug 05, 2024	P128316
G2419478	Certificate of Analysis	Aug 02, 2024	P128316
F2417431	Certificate of Analysis	Jun 26, 2024	P128316
F2417432	Certificate of Analysis	Jun 26, 2024	P128316
F2417409	Certificate of Analysis	Jun 25, 2024	P128316
E2421330	Certificate of Analysis	Jun 04, 2024	P128316
E2421331	Certificate of Analysis	Jun 04, 2024	P128316
E2421332	Certificate of Analysis	Jun 04, 2024	P128316
C2427156	Certificate of Analysis	Apr 07, 2024	P128316
C2427157	Certificate of Analysis	Apr 07, 2024	P128316
C2427158	Certificate of Analysis	Apr 07, 2024	P128316
G2514414	Certificate of Analysis	Mar 30, 2024	P128316
B2422228	Certificate of Analysis	Mar 08, 2024	P128316
B2422229	Certificate of Analysis	Mar 08, 2024	P128316
B2422230	Certificate of Analysis	Mar 08, 2024	P128316
A2412508	Certificate of Analysis	Jan 20, 2024	P128316
A2412509	Certificate of Analysis	Jan 20, 2024	P128316
A2412510	Certificate of Analysis	Jan 20, 2024	P128316
J2325711	Certificate of Analysis	Nov 01, 2023	P128316
J2325709	Certificate of Analysis	Nov 01, 2023	P128316
J2325710	Certificate of Analysis	Nov 01, 2023	P128316
I2313135	Certificate of Analysis	Sep 20, 2023	P128316
I2313151	Certificate of Analysis	Sep 20, 2023	P128316
I2313225	Certificate of Analysis	Sep 20, 2023	P128316
G23151150	Certificate of Analysis	Jul 26, 2023	P128316
G23151152	Certificate of Analysis	Jul 26, 2023	P128316
G2317098	Certificate of Analysis	Jul 26, 2023	P128316
D2325708	Certificate of Analysis	May 13, 2023	P128316
D2325701	Certificate of Analysis	May 12, 2023	P128316
C23161388	Certificate of Analysis	Mar 23, 2023	P128316
C23161317	Certificate of Analysis	Mar 22, 2023	P128316
C23161385	Certificate of Analysis	Mar 22, 2023	P128316
C23161399	Certificate of Analysis	Mar 22, 2023	P128316
B2301287	Certificate of Analysis	Feb 07, 2023	P128316
L2227086	Certificate of Analysis	Jan 05, 2023	P128316
L2227107	Certificate of Analysis	Jan 05, 2023	P128316
L2227117	Certificate of Analysis	Jan 05, 2023	P128316
L2227118	Certificate of Analysis	Jan 05, 2023	P128316
K2217079	Certificate of Analysis	Nov 22, 2022	P128316
K2217129	Certificate of Analysis	Nov 22, 2022	P128316
K2217130	Certificate of Analysis	Nov 22, 2022	P128316
I2215676	Certificate of Analysis	Sep 26, 2022	P128316
I2215677	Certificate of Analysis	Sep 26, 2022	P128316
I2215678	Certificate of Analysis	Sep 26, 2022	P128316
H2212433	Certificate of Analysis	Aug 20, 2022	P128316
B2216475	Certificate of Analysis	Feb 19, 2022	P128316
H2212434	Certificate of Analysis	Feb 19, 2022	P128316
B2216476	Certificate of Analysis	Feb 19, 2022	P128316
B2216477	Certificate of Analysis	Feb 19, 2022	P128316
F2218499	Certificate of Analysis	Feb 19, 2022	P128316
H2212435	Certificate of Analysis	Feb 19, 2022	P128316
F2218497	Certificate of Analysis	Jan 12, 2022	P128316
L2123455	Certificate of Analysis	Jan 12, 2022	P128316

Proprietà chimiche e fisiche

Solubilità	Soluble in water; Degree of Solubility in water: 80 g/l 20 °C; Very soluble in Alcohol,Chloroform,Ether,Acetone; Soluble in Benzene,Methanol
Sensibilità	Light sensitive
Indice di rifrazione	1.54178
Punto di infiammabilità (°F)	177.8 °F - closed cup
Punto di infiammabilità (°C)	79.44℃（closed cup）
Punto di ebollizione (°C)	181.7°C
Punto di fusione (°C)	43°C
Peso molecolare	94.110 g/mol
XLogP3	1.500
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	94.0419 Da
Monoisotopic Mass	94.0419 Da
Topological Polar Surface Area	20.200 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	46.100
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

Domande frequenti e articoli

Application of Magnetic Nanoparticles in RNA and DNA Separation

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MNPs Nanoparticles Silicon dioxide Magnetic material DNA separation RNA isolation

Strategies for Eluting Biotinylated Proteins and Nucleic Acids from Streptavidin Supports

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Streptavidin Biotin

Research Progress in Detection Technologies for Soluble Sugars in Plants

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Soluble sugars

A Review of Ten Commonly Used Techniques for Detection, Quantification, and Interaction Analysis in Nucleic Acid Research

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PCR ChIP EMSA Nucleic acid detection Nucleic acid quantification RT-PCR Sequencing UV spectrophotometry Southern blot Northern blot Nucleic acid probes DNA footprinting

Recent Advances in Methods for Measuring Starch-Related Indices in Plants and Their Application-Oriented Selection

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Spectrophotometry Starch Soluble starch Total starch Amylose Amylopectin Resistant starch Iodine blue value Colorimetric assay

RNA Extraction Technologies: Method Systems, Operational Workflows, and Key Quality-Control Considerations

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RNA extraction RNase Magnetic beads Column-based method organic extraction DNase treatment A260/280 A260/230 RIN

Cholesterol Esterase: Mechanistic Insights and Application Frameworks Driven by Interfacial Hydrolysis

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Biocatalysis cholesterol esteras cholesteryl ester hydrolysis interfacial catalysis bile-salt activation total cholesterol assay lipidomics lipoproteins enzyme immobilization

Lipid Panel Testing in Research (TC, TG, HDL-C, LDL-C): Indicator System, Assay Principles, Technical Routes, and Application Overview

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HPLC lipid panel total cholesterol triglycerides HDL-C LDL-C enzymatic colorimetry homogeneous assays precipitation methods ultracentrifugation calibration interference control

Micrococcal Nuclease (MNase): A Technical Review of Enzymatic Properties, Reaction Control, and Research and Biomanufacturing Applications

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MNase micrococcal nuclease Ca2+ dependence 3′-phosphate termini

Interleukin-29 (IL-29/IFN-λ1): Molecular Features, Signaling Networks, and a Systematic Framework for Research Applications

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JAK-STAT IL-29 IFN-λ1 type III interferon IFNLR1/IL-28RA IL-10RB ISGF3 ISG SOCS USP18 mucosal immunity epithelial barrier antiviral

Physicochemical Properties of Diphenylamine, Analytical Applications, and a Review of Its DNA Colorimetric Reaction

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Quality control Diphenylamine DPA Aromatic amine DNA colorimetric assay Deoxyribose Furfural derivatives Chromogenic reaction

Review of the Principles, Common Methods, and Key Application Considerations for the Determination of Glycerol and Triglyceride Contents

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lipase Methodological standardization Enzymatic Assay Glycerol Triglyceride Glycerol Kinase Glycerol Phosphate Oxidase Chromatographic Analysis Mass Spectrometric Analysis

Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)

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Cross-coupling Haloheterocycles

β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention

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AAAs β-Acyloxy Alkenyl Amides

Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids

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Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity

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ATD-DMAP

Triphenylphosphine Dibromide (PPh₃Br₂) Is More Than Just a Brominating Reagent: Experimental Selection Logic from Alcohol-to-Alkyl Bromide Conversion to Carboxylic Acid Activation and One-Pot Esterification, Vinyl Bromide Formation, and Nitrile Constructi

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carboxylic acid activation Bromide agent

Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway

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DBU Bicyclic amidine reagents

DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization

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Organic synthesis Acyl transfer Organic base Esterification

Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks

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Organic synthesis Triphosgene

Comparative Analysis and Selection Strategies for Mounting Media in Immunological Experiments

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Immunohistochemistry Immunofluorescence mounting medium antifade glycerol gelatin PVP Kisser mounting medium

Formulation Design and Selection of Amine Curing Agents in Epoxy Systems

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Epoxy-Amine Cure

Experimental Decision-Making for Cross-Coupling Reactions: Target Bond Type, Substrate Combination, and Catalytic System Selection

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Cross-coupling Cross-coupling reactions

Adding a Temperature-Triggered Switch to NCO: How Blocked Isocyanates Affect the Storage, Curing, and Film Performance of 1K Baking Coatings

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High-performance polyurethane Isocyanate group

Microscopic Interpretation and Taxonomic Value of Iodine Staining Reaction in Fungal Spores

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IKI Melzer’s reagent Lugol’s iodine Fungal Spores Iodine Reaction Amyloid Reaction Dextrinoid Reaction Spore Wall Spore Ornamentation Fungal Microscopic Identification

1K, 2K, Waterborne, Moisture-Curing, and Blocked Systems: Classification Logic and Identification Methods for Polyurethane Coating Curing Systems

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Polyurethane Coatings Dispersion Medium

Key Control Points in Polyurethane Coating Formulation Design and Application

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Polyurethane Polyurethane Coatings

Microbial Morphological Identification: Observation Systems, Staining Methods, and Result Interpretation

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Gram staining Microbial Morphological Identification Bacterial Morphology Fungal Morphology Acid-Fast Staining Spore Staining Capsule Staining Colony Morphology Microscopic Observation Microbial Quality Control

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Peptide synthesis Abnormal impurities

Why Do Phenolic Resins Have Good Heat and Chemical Resistance? Analyzing the Source of Their Performance from Molecular Structure to Cured Networks

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Coating surface Phenol-Formaldehyde Resin Thermosetting Resin

Epoxy Phenolic Coatings: Why Are They Commonly Used for Chemical Resistance, Solvent Resistance, Heat Resistance, and Internal Metal Surface Protection?

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Epoxy resin Paint Phenolic Resin Phenolic Crosslinking Agent

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Alkyd Resins Paint Industrial Coatings Film-forming resin

Selection and Formulation Design Guidelines for Phenolic Resins in Coatings: Applicable Scenarios, Application Limitations, and Performance Verification

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Phenol-Formaldehyde Resin Paint

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Ink resin Paint Natural resin

Cashew Nut Shell Liquid (CNSL): From Cashew Processing By-Product to Reactive Bio-Based Raw Material for Coating Resins

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Coating Resins Adhesive Rich in phenolic compounds

Choline Metabolism and Detection Methods: Pathway Analysis of Choline, Phosphatidylcholine, Betaine, Acetylcholine, and TMAO

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Acetylcholine betaine phosphatidylcholine LC-MS/MS TMAO Choline Metabolism Choline Detection Choline Oxidase Method

Aladdin® Plant Research Related Products

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Plant tissue culture Genetic transformation Botany Phytohormones Protoplasts Infection

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ABCAs azabicyclo[x.1.1]alkanes

Moisturizing Mechanisms of Tremella fuciformis Polysaccharides: From Polysaccharide Structure and Hydration Rheology to Dynamic Film Formation on the Skin Surface

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Tremella fuciformis Polysaccharides

How to Bypass α-Fluoride Elimination: Bromine-Transfer Capture and Oxidative Coupling of α,α-Difluorobenzylic Anions

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Deprotonation

Phase-Partitioning Principles, System Differences, and Application Selection in Phenol-Based DNA and RNA Extraction

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RNA extraction DNA extraction Quality control phenol-based extraction phenol-chloroform isoamyl alcohol acidic phenol guanidinium thiocyanate liquid-liquid partitioning nucleic acid purification

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

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

Reaction Logic of I₂/DMSO-Mediated Oxidation of Aryl Methyl Ketones: In Situ Generation, Trapping, and Heterocycle Construction of Aryl Glyoxals

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Dimethyl sulfoxide DMSO

From Temporary Covalent Assembly to Intramolecular Smiles Aryl Migration: DCPDC-Mediated Phenol–Primary Amine C–N Cross-Coupling

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Drugs Aryl C–N

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Phenol - ≥99% , CAS No.108-95-2

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Literature proof

Specifications

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📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

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