Chrome blue-black R indicator - 0.2%(w/w)in Sodium chloride , CAS No.2538-85-4

CAS: 2538-85-4 Cat. No.: E196476 Peso molecular: 416.39 Número EC: 219-810-2
Disponible para pedir
GRADE & PURITY 0.2%(w/w)in Sodium chloride
Synonyms
Hispacrom Blue B | NCGC00167429-05 | A0581 | C.I. 15705 | Java Chrome Blue Black RN | S01HA03 | Chrome Fast Cyanine GR | Chromazine Blue Black R | Chrome Fast Cyanine BSS | Pontachrome Blue Black R | 3-Hydroxy-4-(2-hydroxy-1-naphthylazo)-1-naphthalenesulf
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
500g
E196476-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

161,90US$

189,90US$
Guardar 28,00 US$ (14.74%)
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Why this grade

0.2%(w/w)in Sodium chloride for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Hispacrom Blue B | NCGC00167429-05 | A0581 | C.I. 15705 | Java Chrome Blue Black RN | S01HA03 | Chrome Fast Cyanine GR | Chromazine Blue Black R | Chrome Fast Cyanine BSS | Pontachrome Blue Black R | 3-Hydroxy-4-(2-hydroxy-1-naphthylazo)-1-naphthalenesulf
Especificaciones y pureza
0.2%(w/w)in Sodium chloride
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nombres e identificadores
Sonrisas canónicasC1=CC=C2C(=C1)C=CC(=C2N=NC3=C(C=C(C4=CC=CC=C43)S(=O)(=O)[O-])O)O.[Na+]
IUPAC Namesodium;3-hydroxy-4-[(2-hydroxynaphthalen-1-yl)diazenyl]naphthalene-1-sulfonate
InChIKeyZQWICJYATMSSSD-UHFFFAOYSA-M
INCHI1S/C20H14N2O5S.Na/c23-16-10-9-12-5-1-2-6-13(12)19(16)21-22-20-15-8-4-3-7-14(15)18(11-17(20)24)28(25,26)27;/h1-11,23-24H,(H,25,26,27);/q;+1/p-1
Isómeros SMILES C1=CC=C2C(=C1)C=CC(=C2N=NC3=C(C=C(C4=CC=CC=C43)S(=O)(=O)[O-])O)O.[Na+]
Peso molecular 416.39
Reaxy-Rn 6041435
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6041435&ln=

Documentation

📋 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

KingdomOrganic compounds
SuperclassBenzenoids
ClaseNaphthalenes
Subclass1,1'-azonaphthalenes
Intermediate Tree Nodes Not available
Direct Parent1,1'-azonaphthalenes
Alternative Parents 1-naphthalene sulfonic acids and derivatives  1-naphthalene sulfonates  Naphthols and derivatives  1-sulfo,2-unsubstituted aromatic compounds  1-hydroxy-2-unsubstituted benzenoids  Sulfonyls  Organosulfonic acids  Azo compounds  Propargyl-type 1,3-dipolar organic compounds  Organooxygen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Organic cations  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 1,1'-azonaphthalene - Naphthalene sulfonate - 1-naphthalene sulfonic acid or derivatives - Naphthalene sulfonic acid or derivatives - 1-naphthalene sulfonate - 2-naphthol - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Azo compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic alkali metal salt - Organic salt - Organic sodium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic cation - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 1,1'-azonaphthalenes. These are organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to the 1-position of a naphthalene ring system. Naphthalene is a compound made up of two fused benzene rings.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular416.400 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass416.044 Da
Monoisotopic Mass416.044 Da
Topological Polar Surface Area131.000 Ų
Heavy Atom Count29
Formal Charge0
Complexity685.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Junli Zheng, Linlin Du, Peng Gao, Kaiwei Chen, LiLi Ma, Yuanli Liu, Shaohong You.  (2021)  Mino-modified biomass for highly efficient removal of anionic dyes from aqueous solutions.  Journal of the Taiwan Institute of Chemical Engineers,      [PMID:] [10.1016/j.jtice.2021.01.026]
2. Xiaoping Wang, Chao Wu, Tongren Zhu, Pan Li, Shengji Xia.  (2020)  The hierarchical flower-like MoS2 nanosheets incorporated into PES mixed matrix membranes for enhanced separation performance.  CHEMOSPHERE,      [PMID:32470733] [10.1016/j.chemosphere.2020.127099]
3. Xinxin Yu, Meng Xia, Qiuyi Bao, Zhihuan Xiao, Yuzhen Zhao, Mingzhong Wei, Yongpeng Li, Zhuyin Sui, Qi Chen.  (2025)  Ultrasonically engineered bionic porous nanofiber evaporator for solar-driven photothermal–photocatalytic synergy in desalination and dye degradation.  DESALINATION,      [PMID:] [10.1016/j.desal.2025.119762]
Calculadoras de soluciones
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