8-hydroxyquinoléines - AR, ≥99% , CAS No.148-24-3

CAS: 148-24-3 Cat. No.: H104638 Formule: C₉H₇NO Poids moléculaire: 145.16 Beilstein Registry Number: 114512 Numéro CE: 205-711-1

QUALITÉ & PURETÉ AR, ≥99%

Synonyms

Oxine|o-Oxychinolin|o-Oxychinolin [German]|Oxine;8-Hydroxyquinoline;Quinophenol;8-Quinolinone|8-Hydroxyquinoline Oxine|Oxychinoline|8-Chinolinol [Czech]|8-HYDROXYQUINOLINE (IARC)|Hydroxybenzopyridine|8 Hydroxyquinoline|8-hydroxiquinoline|Oxyquinoline [USAN]|Tumex|8-Oxyquinoline|Oxybenzopyridine|8-HYDROXYQUINOLINE|8-hydroxy-quinoline|8-Hydroxy-chinolin [German]|8-HYDROXYQUINOLINE [IARC]|8-quinolinol|Quinoline, 8-hydroxy-|HYDROXYQUINOLINE|OXYQUINOLINE (II)|Bioquin|1-Azanaphthalene-8-ol|8-Oxyquinolin|Oxyquinoline|Pesticide Code: 059803|UDDER BALM|8-Quinol|8-Quinolinone|OXYQUINOLINE [VANDF]|8-Chinolinol|8-OQ|quinoline-8-ol|8-Quinolol|8-Hydroxychinolin|8-Hydroxy-chinolin|Phenopyridine|8 Quinolinol|8-hydroxychinoline|quinolin-8-ol|OXYQUINOLINE [HSDB]|OXYQUINOLINE [INCI]|Fennosan HF-15|Oxin|Usaf ek-794|Oxyquinoline (8-Hydroxyquinoline)|Quinophenol|Oxyquinol|8-hydroxylquinoline|Manganese, bis(8-quinolinolato)-|Fennosan H 30|HQY|Oxyquinoline (USAN)|OXYQUINOLINE [II]|8-hydroxy quinoline|8-Oxychinolin|Oxoquinoline

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Vue d’ensemble

la réaction de la 8-hydroxyquinoline avec l'aluminium(III) produit l'Alq3, un composant commun des diodes électroluminescentes organiques (OLED). Les variations des substituants sur les anneaux de quinoléine affectent ses propriétés luminescentes. la 8-hydroxyquinoléine est utilisée pour la précipitation et la séparation des métaux, la préparation de fongicides et comme colorant
Utilisée comme agent chélateur lipophile monoprotique bidentate.

Spécifications

Synonymes

Oxine | o-Oxychinolin | o-Oxychinolin [German] | Oxine;8-Hydroxyquinoline;Quinophenol;8-Quinolinone | 8-Hydroxyquinoline Oxine | Oxychinoline | 8-Chinolinol [Czech] | 8-HYDROXYQUINOLINE (IARC) | Hydroxybenzopyridine | 8 Hydroxyquinoline | 8-hydroxiquinoline | Oxyquinoline [USAN] | Tumex | 8-Oxyquinoline | Oxybenzopyridine | 8-HYDROXYQUINO Afficher plus

Spécifications et pureté

AR, ≥99%

Mécanismes biochimiques et physiologiques

Inhibiteur de la synthèse de l'ARN agissant comme fongicide contre Trichophyton mentagrophytes, Myrothecium verrucaria et Trichoderma viride. Le mécanisme d'action antifongique n'est pas clair mais semble être structurellement lié à l'inhibiteur de la syn

Conditions de stockage de stockage

Protected from light,Argon charged,Room temperature

Expédié en

Normal

Grade

AR

Note

Dans la mesure du possible, les solutions doivent être préparées et utilisées le même jour. Toutefois, si vous devez préparer des solutions de base à l'avance, nous vous recommandons de les conserver sous forme d'aliquotes dans des flacons hermétiques à -20°C. Ces aliquotes sont généralement utilisables pendant un mois. En général, ces solutions peuvent être utilisées pendant un mois. Avant utilisation, et avant d'ouvrir le flacon, nous vous recommandons de laisser votre produit s'équilibrer à la température ambiante pendant au moins 1 heure. Toxique, se référer à la FDS pour plus d'informations Vous avez besoin de plus de conseils sur la solubilité, l'utilisation et la manipulation ? Veuillez consulter notre page de questions fréquemment posées (FAQ) pour plus de détails.

Pureté

≥99%

Noms et identifiants

Pubchem Sid

488179645

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488179645

Sourires canoniques

C1=CC2=C(C(=C1)O)N=CC=C2

IUPAC Name

quinolin-8-ol

InChIKey

MCJGNVYPOGVAJF-UHFFFAOYSA-N

INCHI

1S/C9H7NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H

Isomères SMILES

C1=CC2=C(C(=C1)O)N=CC=C2

WGK Allemagne

3

RTECS

VC4200000

Numéro ONU

2811

Groupe d'emballage

I

Poids moléculaire

145.16

Beilstein

114512

Reaxy-Rn

114512

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114512&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Quinolines and derivatives
      • Subclass 8-hydroxyquinolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Quinolines and derivatives
• Subclass: 8-hydroxyquinolines
• Intermediate Tree Nodes: Not available
• Direct Parent: 8-hydroxyquinolines
• Alternative Parents: 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Pyridines and derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 8-hydroxyquinoline - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as 8-hydroxyquinolines. These are compounds containing a quinoline moiety, which carries a hydroxy group at the 8-position. Quinoline consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.
• External Descriptors: a small molecule

Data sources

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

Cibles associées (humaines)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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F2 Tclin Thrombin (11687 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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

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

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ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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TYR Tclin Tyrosinase (717 Activities)

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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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COMT Tclin Catechol O-methyltransferase (404 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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

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

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

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

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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CALCR Tclin Calcitonin receptor (2215 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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

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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

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Cibles associées (non humaines)

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

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Ltc4s Leukotriene C4 synthase (1 Activities)

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Sigmar1 Sigma opioid receptor (160 Activities)

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Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Mapk1 MAP kinase ERK2 (650 Activities)

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Mmp2 Matrix metalloproteinase-2 (12 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Galc Galactocerebrosidase (11 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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HD1 Histone deacetylase (38 Activities)

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npr Thermolysin (425 Activities)

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Streptococcus pneumoniae (31063 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Staphylococcus aureus (210822 Activities)

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Escherichia coli (133304 Activities)

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Streptococcus mutans (2687 Activities)

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Mycobacterium tuberculosis (203094 Activities)

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Saccharomyces cerevisiae (19171 Activities)

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Enterococcus faecalis (29875 Activities)

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Plasmodium falciparum (966862 Activities)

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Candida albicans (78123 Activities)

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Nakaseomyces glabratus (9108 Activities)

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Candida tropicalis (8381 Activities)

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Toxoplasma gondii (4585 Activities)

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Rattus norvegicus (775804 Activities)

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Salmonella enterica (1497 Activities)

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FM3A (1296 Activities)

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P388 (20296 Activities)

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Vero (26788 Activities)

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ScN2a (522 Activities)

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Bacterial leucyl aminopeptidase (60 Activities)

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lef Anthrax lethal factor (7585 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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botA Botulinum neurotoxin type A (1303 Activities)

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Brain (1 Activities)

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

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fba Fructose-bisphosphate aldolase (8 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

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NS1 Nonstructural protein 1 (33327 Activities)

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Glra2 Glycine receptor (1745 Activities)

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SARS-CoV-2 (38078 Activities)

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Burkholderia thailandensis (182 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in acetone, ethanol, chloroform, and benzene. Insoluble in water
• Sensibilité: Light sensitive.Air sensitive
• Point d'ébullition (°C): 266.6°C
• Point de fusion (°C): 76°C
• Poids moléculaire: 145.160 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 145.053 Da
• Monoisotopic Mass: 145.053 Da
• Topological Polar Surface Area: 33.100 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 138.000
• 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

Foire aux questions

What is the purity of this product?

This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

What does AR mean?

AR is a defined analytical purity tier suitable for general analytical and reagent applications. It specifies a minimum assay percentage, controlled limits on common impurities (water, heavy metals, residue on ignition), and lot-to-lot consistency. AR is one of several purity tiers — choose based on the sensitivity and regulatory requirements of your method.

How should this product be stored?

Store at room temperature, protected from light, under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 148-24-3, the molecular formula is C9H7NO, and the molecular weight is 145.16 g/mol. InChIKey MCJGNVYPOGVAJF-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.