N,N-Diethyl-p-phenylenediamine sulfate salt - AR, ≥98% , CAS No.6283-63-2

CAS: 6283-63-2 Cat. No.: A106039 Molecular Weight: 262.33 Beilstein Registry Number: 4219768 EC Number: 228-500-6
AVAILABLE TO ORDER
GRADE & PURITY AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥98%
Synonyms
1,4-Benzenediamine, N,N-diethyl-, sulfate | N,N-Diethyl-benzene-1,4-diamine sulfate | N,N-DIETHYLBENZENE-1,4-DIAMINE SULFATE | FD10478 | N,N-Diethyl-p-phenylenediamine sulfate (VAN) | N1,N1-diethylbenzene-1,4-diaminexsulfate | N,N-Diethyl-1,4-benzenediami
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
A106039-5g
≥10

$9.90

$14.90
Save $5.00 (33.56%)
25g
A106039-25g
≥10

$15.90

$23.90
Save $8.00 (33.47%)
100g
A106039-100g
≥10

$35.90

$53.90
Save $18.00 (33.40%)
500g
A106039-500g
3

$152.90

$229.90
Save $77.00 (33.49%)
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Why this grade

AR, ≥98% AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 49 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
1, 4-Benzenediamine, N, N-diethyl-, sulfate | N, N-Diethyl-benzene-1, 4-diamine sulfate | N, N-DIETHYLBENZENE-1, 4-DIAMINE SULFATE | FD10478 | N, N-Diethyl-p-phenylenediamine sulfate (VAN) | N1, N1-diethylbenzene-1, 4-diaminexsulfate | N, N-Diethyl-1, 4-benzenediami
Specifications & Purity
AR, ≥98%
Storage
Argon charged, Room temperature
Shipped In
Normal
Grade
AR
Purity
≥98%
Names and Identifiers
Pubchem Sid488185820
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185820
Canonical SmilesCCN(CC)C1=CC=C(C=C1)N.OS(=O)(=O)O
IUPAC Name4-N,4-N-diethylbenzene-1,4-diamine;sulfuric acid
InChIKeyAYLDJQABCMPYEN-UHFFFAOYSA-N
INCHI1S/C10H16N2.H2O4S/c1-3-12(4-2)10-7-5-9(11)6-8-10;1-5(2,3)4/h5-8H,3-4,11H2,1-2H3;(H2,1,2,3,4)
Isomeric SMILES CCN(CC)C1=CC=C(C=C1)N.OS(=O)(=O)O
WGK Germany 3
RTECS SS9625000
Alternate CAS 6065-27-6
Molecular Weight 262.33
Beilstein 4219768
Reaxy-Rn 4219768
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4219768&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClassOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Tertiary amines - Tertiary alkylarylamines
Direct ParentDialkylarylamines
Alternative Parents Aniline and substituted anilines  Organic sulfuric acids  Primary amines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Dialkylarylamine - Sulfuric acid - Benzenoid - Monocyclic benzene moiety - Organic sulfuric acid or derivatives - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
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.

36 results found

Lot NumberCertificate TypeDateItem
D2622115Certificate of AnalysisMay 06, 2026 A106039
G2230394Certificate of AnalysisApr 27, 2026 A106039
G2230395Certificate of AnalysisApr 27, 2026 A106039
G2230393Certificate of AnalysisApr 27, 2026 A106039
D2609089Certificate of AnalysisApr 22, 2026 A106039
C2219126Certificate of AnalysisJan 19, 2026 A106039
C2219115Certificate of AnalysisJan 19, 2026 A106039
C2219111Certificate of AnalysisJan 19, 2026 A106039
C2219100Certificate of AnalysisJan 19, 2026 A106039
C2205154Certificate of AnalysisDec 12, 2025 A106039
C2204114Certificate of AnalysisDec 10, 2025 A106039
C2204128Certificate of AnalysisDec 10, 2025 A106039
C2204113Certificate of AnalysisDec 10, 2025 A106039
C2204070Certificate of AnalysisDec 10, 2025 A106039
B2219036Certificate of AnalysisDec 10, 2025 A106039
B2218180Certificate of AnalysisDec 10, 2025 A106039
B2218168Certificate of AnalysisDec 10, 2025 A106039
B2218149Certificate of AnalysisDec 10, 2025 A106039
B2218148Certificate of AnalysisDec 10, 2025 A106039
K2119063Certificate of AnalysisSep 04, 2025 A106039
K2119061Certificate of AnalysisSep 04, 2025 A106039
K2119062Certificate of AnalysisSep 04, 2025 A106039
K2119060Certificate of AnalysisSep 04, 2025 A106039
A2118098Certificate of AnalysisNov 05, 2024 A106039
K2219010Certificate of AnalysisOct 18, 2022 A106039
K2219009Certificate of AnalysisOct 18, 2022 A106039
K2219044Certificate of AnalysisOct 18, 2022 A106039
K2219047Certificate of AnalysisOct 18, 2022 A106039
A2415036Certificate of AnalysisOct 18, 2022 A106039
I2528074Certificate of AnalysisOct 18, 2022 A106039
A2415101Certificate of AnalysisOct 18, 2022 A106039
J2531086Certificate of AnalysisJan 03, 2022 A106039
I2528069Certificate of AnalysisJan 03, 2022 A106039
H2428034Certificate of AnalysisJan 03, 2022 A106039
G2303591Certificate of AnalysisJan 03, 2022 A106039
L2503077Certificate of AnalysisJan 03, 2022 A106039

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Chemical and Physical Properties
SolubilitySoluble in water and alcohol.
SensitivityAir sensitive.Light sensitive.
Melt Point(°C)184-186°C
Molecular Weight262.330 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass262.099 Da
Monoisotopic Mass262.099 Da
Topological Polar Surface Area112.000 Ų
Heavy Atom Count17
Formal Charge0
Complexity194.000
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
Citations of This Product
References
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18. Tao Li, Lin Dai, Yixin Huang, Siwen Pan, Zijun Pang, Jing Zou.  (2021)  Spectrophotometric determination of Cr(VI) in water using N,N-diethyl-p-phenylenediamine (DPD) as the indicator.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2021.105517]
19. Zijun Pang, Yajuan Cai, Weihao Xiong, Junyang Xiao, Jing Zou.  (2020)  A spectrophotometric method for measuring permanganate index (CODMn) by N,N-diethyl-p-phenylenediamine (DPD).  CHEMOSPHERE,      [PMID:33223208] [10.1016/j.chemosphere.2020.128936]
20. Wanjun Wang, Wenquan Gu, Guiying Li, Haojing Xie, Po Keung Wong, Taicheng An.  (2020)  Few-layered tungsten selenide as a co-catalyst for visible-light-driven photocatalytic production of hydrogen peroxide for bacterial inactivation.  Environmental Science-Nano,  (12): (3877-3887).  [PMID:] [10.1039/D0EN00801J]
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23. Guilin He, Tuqiao Zhang, Feifei Zheng, Cong Li, Qingzhou Zhang, Feilong Dong, Yuan Huang.  (2019)  Reaction of fleroxacin with chlorine and chlorine dioxide in drinking water distribution systems: Kinetics, transformation mechanisms and toxicity evaluations.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.06.022]
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44. Shuang Liu, Chao Liu, Hejiao Zhang, Weizhen Zhang, Wei Ding, Huaili Zheng, Hong Li.  (2024)  Sulfite induced degradation of sulfamethoxazole by a silica stabilized ZIF-67(Co) catalyst via non-radical pathways: Formation and role of high-valent Co(IV) and singlet oxygen.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:38412645] [10.1016/j.jhazmat.2024.133888]
45. Zhaofen Xu, Lingfang Tang, Yuanyi Zhou, Gang Lu, Haojie Dong, Mingshan Zhu.  (2024)  Utilizing the immanent chloride ions in wastewater for reactive chlorine species photogeneration towards effective ammonia nitrogen removal.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.152589]
46. Ying Xu, Cong Dai, Zhifeng Xu.  (2025)  Dual-channel ratiometric sensing of hypochlorous acid based on organic cage with red and green fluorescence.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40945009] [10.1016/j.saa.2025.126928]
47. Li Yongqiang, Yang Siwei, Bao Wancheng, Tao Quan, Jiang Xiuyun, Li Jipeng, He Peng, Wang Gang, Qi Kai, Dong Hui, Ding Guqiao, Xie Xiaoming.  (2024)  Accelerated proton dissociation in an excited state induces superacidic microenvironments around graphene quantum dots.  Nature Communications,  15  (1): (1-13).  [PMID:39103388] [10.1038/s41467-024-50982-x]
48. Jiabao Wu, Meiyu Xu, Bo Wang, Lijun Liao, Mingxia Li, Wei Zhou.  (2025)  Insight into the synergistic effect of oxygen vacancy defects and intimate interfaces in Ni/NiTiO3 for full solar spectrum-driven H2O2 production.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.163825]
49. Rongjiao Tan, Bingguang Zhang, Xianghong Li, Changjun Yang, Dingguo Tang, Kejian Deng.  (2025)  Photocatalytic activity of asymmetric cobalt thioporphyrazine for selective aerobic oxidation of amines under visible light.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2025.120618]
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