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Azomethine H - 97%, high purity , CAS No.5941-07-1

    Grade & Purity:
  • ≥97%
In stock
Item Number
A109399
Grouped product items
SKU Size
Availability
Price Qty
A109399-1g
1g
5
$19.90
A109399-5g
5g
3
$74.90
View related series
Spectroscopic reagent (233)

Basic Description

Synonyms AKOS040760036 | Azomethine-H (monosodium) | Azomethine-H Monosodium Salt | PD158026 | HY-D0797 | SODIUM (E)-4-HYDROXY-5-((2-HYDROXYBENZYLIDENE)AMINO)-7-SULFONAPHTHALENE-2-SULFONATE | sodium (E)-4-hydroxy-5-(2-hydroxybenzylideneamino)-7-sulfonaphthalene-2-
Specifications & Purity ≥97%
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Naphthalenes
Subclass Naphthalene sulfonic acids and derivatives
Intermediate Tree Nodes Naphthalene sulfonates
Direct Parent 2-naphthalene sulfonates
Alternative Parents 2-naphthalene sulfonic acids and derivatives  Naphthols and derivatives  1-sulfo,2-unsubstituted aromatic compounds  Phenoxides  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Sulfonyls  Organosulfonic acids  Shiff bases  Propargyl-type 1,3-dipolar organic compounds  Organooxygen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Organic cations  
Molecular Framework Aromatic homopolycyclic compounds
Substituents 2-naphthalene sulfonic acid or derivatives - 2-naphthalene sulfonate - 1-naphthol - 1-sulfo,2-unsubstituted aromatic compound - Arylsulfonic acid or derivatives - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Phenoxide - 1-hydroxy-4-unsubstituted benzenoid - Monocyclic benzene moiety - Organic sulfonic acid or derivatives - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Shiff base - Organic alkali metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Aldimine - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organic sodium salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Imine - Organic oxide - Organic cation - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as 2-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 2-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors Not available

Associated Targets(Human)

A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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NCI-H322M (45589 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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NCI-H460 (60772 Activities)
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SF-268 (49410 Activities)
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IGROV-1 (47897 Activities)
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LOX IMVI (44321 Activities)
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HOP-62 (47048 Activities)
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MDA-MB-435 (38290 Activities)
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MDA-N (28205 Activities)
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Malme-3M (44254 Activities)
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MDA-MB-231 (73002 Activities)
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Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488203008
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488203008
IUPAC Name sodium;4-hydroxy-5-[(2-hydroxyphenyl)methylideneamino]-7-sulfonaphthalene-2-sulfonate
INCHI InChI=1S/C17H13NO8S2.Na/c19-15-4-2-1-3-10(15)9-18-14-7-12(27(21,22)23)5-11-6-13(28(24,25)26)8-16(20)17(11)14;/h1-9,19-20H,(H,21,22,23)(H,24,25,26);/q;+1/p-1
InChIKey VDMRMECRCLGIAD-UHFFFAOYSA-M
Smiles C1=CC=C(C(=C1)C=NC2=C3C(=CC(=C2)S(=O)(=O)O)C=C(C=C3O)S(=O)(=O)[O-])O.[Na+]
Isomeric SMILES C1=CC=C(C(=C1)C=NC2=C3C(=CC(=C2)S(=O)(=O)O)C=C(C=C3O)S(=O)(=O)[O-])O.[Na+]
WGK Germany 3
Alternate CAS 206752-32-1
Molecular Weight 445.39
Reaxy-Rn 4100175
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4100175&ln=

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.

8 results found

Lot Number Certificate Type Date Item
D2008046 Certificate of Analysis Jan 15, 2024 A109399
E2327046 Certificate of Analysis Apr 23, 2023 A109399
E2327044 Certificate of Analysis Apr 23, 2023 A109399
E2327050 Certificate of Analysis Apr 23, 2023 A109399
E2327057 Certificate of Analysis Apr 23, 2023 A109399
B2325335 Certificate of Analysis May 14, 2022 A109399
F2206056 Certificate of Analysis May 14, 2022 A109399
F2206061 Certificate of Analysis May 14, 2022 A109399

Chemical and Physical Properties

Solubility Soluble in water.
Molecular Weight 445.400 g/mol
XLogP3
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 9
Rotatable Bond Count 4
Exact Mass 444.99 Da
Monoisotopic Mass 444.99 Da
Topological Polar Surface Area 181.000 Ų
Heavy Atom Count 29
Formal Charge 0
Complexity 791.000
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 2

Citations of This Product

1. Xiaowei Liu, Qingxiao Lu, Qikun Zhou, Peng Chen, Kexin Li.  (2023)  Bisulfite-activated permanganate oxidation plus coagulation as a pretreatment of SWRO desalination lines to enhance boron rejection.  SEPARATION AND PURIFICATION TECHNOLOGY,  308  (122959). 

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