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Diphenyl guanidine - 97%, high purity , CAS No.102-06-7

11 Citations COA COA
    Grade & Purity:
  • ≥97%
In stock
Item Number
D109220
Grouped product items
SKU Size
Availability
 Price Qty
D109220-1g
1g
3
$9.90
D109220-5g
5g
3
$12.90
D109220-25g
25g
3
$17.90
D109220-100g
100g
3
$20.90
D109220-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$36.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms 1,3-Diphenylguanidine | CAS-102-06-7 | F3096-1727 | phenax | Tox21_110998 | Tox21_110998_1 | Tox21_400041 | Cambridge id 5539652 | NSC3272NSC 3272 | 1,3-Difenylguanid [Czech] | Denax DPG | Vanax DPG | NCGC00090698-06 | HMS548O11 | 1,3-Difenylguanid | FT-0
Specifications & Purity ≥97%
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Benzene and substituted derivatives
Alternative Parents Guanidines  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Monocyclic benzene moiety - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors Not available

Associated Targets(Human)

SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 (4 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trpc4 Short transient receptor potential channel 4 (1615 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

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 504751400
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504751400
IUPAC Name 1,2-diphenylguanidine
INCHI InChI=1S/C13H13N3/c14-13(15-11-7-3-1-4-8-11)16-12-9-5-2-6-10-12/h1-10H,(H3,14,15,16)
InChIKey OWRCNXZUPFZXOS-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)NC(=NC2=CC=CC=C2)N
Isomeric SMILES C1=CC=C(C=C1)NC(=NC2=CC=CC=C2)N
WGK Germany 2
RTECS MF0875000
UN Number 3077
Packing Group III
Molecular Weight 211.26
Beilstein 1875653
Reaxy-Rn 642243
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=642243&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.

13 results found

Lot Number Certificate Type Date Item
B2119563 Certificate of Analysis Dec 05, 2024 D109220
C2531140 Certificate of Analysis Jul 29, 2024 D109220
C2531138 Certificate of Analysis Jul 29, 2024 D109220
C2531139 Certificate of Analysis Jul 29, 2024 D109220
G2404178 Certificate of Analysis Apr 28, 2024 D109220
G2404177 Certificate of Analysis Apr 28, 2024 D109220
F1919051 Certificate of Analysis Apr 11, 2023 D109220
A1921024 Certificate of Analysis Nov 15, 2022 D109220
G2403027 Certificate of Analysis Dec 13, 2021 D109220
D2411063 Certificate of Analysis Dec 13, 2021 D109220
F23161077 Certificate of Analysis Dec 13, 2021 D109220
F23161089 Certificate of Analysis Dec 13, 2021 D109220
F23161093 Certificate of Analysis Dec 13, 2021 D109220

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Chemical and Physical Properties

Solubility Slightly soluble in water, insoluble in gasoline, soluble in ethanol, chloroform, acetone, methanol, and xylene.
Melt Point(°C) 150°C
Molecular Weight 211.260 g/mol
XLogP3 2.400
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 3
Exact Mass 211.111 Da
Monoisotopic Mass 211.111 Da
Topological Polar Surface Area 50.400 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 225.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Xu Han, Wenke Li, Yumei Ji, Lianfeng Wu, Yike Yang, Feng Liu.  (2023)  Strengthening the mechanical properties of polysulfide adhesives by introducing polyurethane.  JOURNAL OF APPLIED POLYMER SCIENCE,  141  (12): (e55123). 
2. Jinbin Lai, Ting Tang, Xiaodong Du, Rui Wang, Jiahao Liang, Dehao Song, Zhi Dang, Guining Lu.  (2023)  Oxidation of 1,3-diphenylguanidine (DPG) by goethite activated persulfate: Mechanisms, products identification and reaction sites prediction.  ENVIRONMENTAL RESEARCH,  232  (116308). 
3. Yanping Wu, Jia Dong, Congzhi Sun, Jinlong Li, Jianmin Chen.  (2020)  A novel methodology for evaluating wear behavior of rubber composites under combination of sliding and rolling conditions.  POLYMER ENGINEERING AND SCIENCE,  60  (9): (2122-2132). 
4. Jing Wang, Hongqiang Li, Lin Zhang, Xuejun Lai, Wenjian Wu, Xingrong Zeng.  (2018)  In situ preparation of reduced graphene oxide reinforced acrylic rubber by self-assembly.  JOURNAL OF APPLIED POLYMER SCIENCE,  136  (11): (47187). 
5. Yanping Wu, Jia Dong, Rui Yuan, Hongqi Wan, Lei Chen, Jinlong Li, Huidi Zhou, Jianmin Chen.  (2018)  Investigate on mechanical and tribological properties of solution styrene butadiene and butadiene rubber composites.  POLYMERS FOR ADVANCED TECHNOLOGIES,  29  (10): (2674-2682). 
6. Yanping Wu, Lei Chen, Songlv Qin, Jinlong Li, Huidi Zhou, Jianmin Chen.  (2017)  Functionalized graphene-reinforced rubber composite: Mechanical and tribological behavior study.  JOURNAL OF APPLIED POLYMER SCIENCE,  134  (25):  
7. Yanping Wu, Lei Chen, Jinlong Li, Huidi Zhou, Haichao Zhao, Jianmin Chen.  (2017)  Understanding the mechanical and tribological properties of solution styrene butadiene rubber composites based on partially graphene oxide.  EUROPEAN POLYMER JOURNAL,  89  (150). 
8. Yanping Wu, Yang Zhou, Jinlong Li, Huidi Zhou, Haichao Zhao, Jianmin Chen.  (2016)  Influence of fillers dispersion on friction and wear performance of solution styrene butadiene rubber composites.  JOURNAL OF APPLIED POLYMER SCIENCE,  133  (26):  
9. Y.P. Wu, Y. Zhou, J.L. Li, H.D. Zhou, J.M. Chen, H.C. Zhao.  (2016)  A comparative study on wear behavior and mechanism of styrene butadiene rubber under dry and wet conditions.  WEAR,  356-357  (1). 
10. Xu Han, Zhijian Pan, Le Chang, Yumei Ji, Zeqian Wang, Feng Liu.  (2024)  Effect of Hard Segment Content and Molecular Weight of Liquid Polysulfide on the Microphase Separation Structure–Property of One-Component Polysulfide Adhesives.  JOURNAL OF APPLIED POLYMER SCIENCE,    (e56577). 
11. Xiaoye Li, Huamin Liu, Yuanyuan Xue, Yanchao Zhu, Juntao Li, Xinyao Li, Shuang Gao.  (2024)  Study on properties of natural latex foam composites modified by corn straw-derived biomass fiber.  POLYMER ENGINEERING AND SCIENCE,     

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