Sodium 5-(2-Aminoethylamino)-1-naphthalenesulfonate Hydrate - ≥98%(HPLC) , CAS No.100900-07-0

CAS: 100900-07-0 Cat. No.: S161259 Molecular Weight: 288.3 EC Number: 622-907-6 PubChem CID: 4116252
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(HPLC)
Synonyms
N-(2-Aminoethyl)-5-naphthylamine-1-sulfonic Acid Sodium Salt | sodium 5-[(2-aminoethyl)amino]naphthalene-1-sulfonate | N-(Aminoethyl)-5-naphthylamine-1-sulfonic Acid Sodium Salt | sodium;5-(2-aminoethylamino)naphthalene-1-sulfonate | AKOS015910596 | Sodiu
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
100mg
S161259-100mg
3

$55.90

$83.90
Save $28.00 (33.37%)
250mg
S161259-250mg
2

$123.90

$185.90
Save $62.00 (33.35%)
1g
S161259-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$446.90

$670.90
Save $224.00 (33.39%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

EDANS, acid and its sodium salt are the most popular donors for developing FRET-based nucleic acid probes that is widely used in real time PCR assays. In addition, it is also used for developing protease substrates. EDANS, sodium salt is often paired with DABCYL or DABSYL in FRET-based probes. Its fluorescence is environment-sensitive.

Specifications

Synonyms
N-(2-Aminoethyl)-5-naphthylamine-1-sulfonic Acid Sodium Salt | sodium 5-[(2-aminoethyl)amino]naphthalene-1-sulfonate | N-(Aminoethyl)-5-naphthylamine-1-sulfonic Acid Sodium Salt | sodium;5-(2-aminoethylamino)naphthalene-1-sulfonate | AKOS015910596 | Sodiu
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Water soluble, blue-green fluorogenic labelling reagent for protein and carbohydrate modifications. EDANS-DABCYL fluorophore-quencher pair is commonly used as a resonance energy transfer pair for peptidase substrate (FRET) analysis.
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note
Refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%(HPLC)
Names and Identifiers
Pubchem Sid504762852
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504762852
Canonical SmilesC1=CC2=C(C=CC=C2S(=O)(=O)[O-])C(=C1)NCCN.[Na+]
IUPAC Namesodium;5-(2-aminoethylamino)naphthalene-1-sulfonate
InChIKeyHGWRACRQRUQQGH-UHFFFAOYSA-M
INCHI1S/C12H14N2O3S.Na/c13-7-8-14-11-5-1-4-10-9(11)3-2-6-12(10)18(15,16)17;/h1-6,14H,7-8,13H2,(H,15,16,17);/q;+1/p-1
Isomeric SMILES C1=CC2=C(C=CC=C2S(=O)(=O)[O-])C(=C1)NCCN.[Na+]
PubChem CID 4116252
Molecular Weight 288.3
Reaxy-Rn 4283850

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
ClassNaphthalenes
SubclassNaphthalene sulfonic acids and derivatives
Intermediate Tree Nodes Naphthalene sulfonates
Direct Parent1-naphthalene sulfonates
Alternative Parents 1-naphthalene sulfonic acids and derivatives  1-sulfo,2-unsubstituted aromatic compounds  Secondary alkylarylamines  Sulfonyls  Organosulfonic acids  Organic zwitterions  Organic sodium salts  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 1-naphthalene sulfonate - 1-naphthalene sulfonic acid or derivatives - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Secondary aliphatic/aromatic amine - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Secondary amine - Organic alkali metal salt - Amine - Organic zwitterion - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 1-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

3 results found

Lot NumberCertificate TypeDateItem
D2110355Certificate of AnalysisJan 06, 2025 S161259
D2110356Certificate of AnalysisJan 06, 2025 S161259
D2110357Certificate of AnalysisJan 06, 2025 S161259
Chemical and Physical Properties
SensitivityAir & Light & Heat sensitive
Molecular Weight288.300 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass288.054 Da
Monoisotopic Mass288.054 Da
Topological Polar Surface Area104.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity372.000
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
Documents & Articles
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.