4-Dietilaminobenzaldehídos - ≥98% , CAS No.120-21-8

CAS: 120-21-8 Cat. No.: D104213 Peso molecular: 177.24 Beilstein Registry Number: 511102 Número EC: 204-377-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Benzaldehyde, p-(diethylamino)- | DIETHYLAMINOBENZALDEHYDE, P- | 4-(Diethylamino)benzaldehyde | 4-(Diethylamino)-Benzaldehyde | 4-N,N-Diethylamino benzaldehyde | InChI=1/C11H15NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-9H,3-4H2,1-2H | AKOS000118909 | p-N,N-d
Storage
Conservar a 2-8°C,cargado con argón
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
D104213-25g
3

21,90US$

32,90US$
Guardar 11,00 US$ (33.43%)
100g
D104213-100g
3

41,90US$

62,90US$
Guardar 21,00 US$ (33.39%)
500g
D104213-500g
1

65,90US$

98,90US$
Guardar 33,00 US$ (33.37%)
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Conservar a 2-8°C,cargado con argón Ships Hielo húmedo 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 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Benzaldehyde, p-(diethylamino)- | DIETHYLAMINOBENZALDEHYDE, P- | 4-(Diethylamino)benzaldehyde | 4-(Diethylamino)-Benzaldehyde | 4-N, N-Diethylamino benzaldehyde | InChI=1/C11H15NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-9H, 3-4H2, 1-2H | AKOS000118909 | p-N, N-d
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C, cargado con argón
Enviado en
Hielo húmedo
Tipo de acción
INHIBITOR
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504754118
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754118
Sonrisas canónicasCCN(CC)C1=CC=C(C=C1)C=O
IUPAC Name4-(diethylamino)benzaldehyde
InChIKeyMNFZZNNFORDXSV-UHFFFAOYSA-N
INCHI1S/C11H15NO/c1-3-12(4-2)11-7-5-10(9-13)6-8-11/h5-9H,3-4H2,1-2H3
Isómeros SMILES CCN(CC)C1=CC=C(C=C1)C=O
WGK Alemania 2
RTECS CU5612850
Número ONU 3077
Peso molecular 177.24
Beilstein 511102
Reaxy-Rn 511102
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=511102&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
ClaseBenzene and substituted derivatives
SubclassBenzoyl derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoyl derivatives
Alternative Parents Dialkylarylamines  Benzaldehydes  Aniline and substituted anilines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzaldehyde - Benzoyl - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Aryl-aldehyde - Tertiary amine - Organic oxide - Aldehyde - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
External Descriptors tertiary amino compound - aromatic amine - benzaldehydes
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ALDH1A1 Tchem Retinal dehydrogenase 1 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALDH2 Tclin Aldehyde dehydrogenase (509 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH3A1 Tchem Aldehyde dehydrogenase dimeric NADP-preferring (307 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A3 Tchem Aldehyde dehydrogenase 1A3 (336 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

7 results found

Lot NumberCertificate TypeFechaArticulo
I2007249Certificate of AnalysisJan 26, 2026 D104213
A2616150Certificate of AnalysisJan 23, 2026 D104213
I2007250Certificate of AnalysisJan 19, 2026 D104213
F2208270Certificate of AnalysisDec 22, 2025 D104213
F2208271Certificate of AnalysisDec 22, 2025 D104213
G2510021Certificate of AnalysisJul 17, 2025 D104213
G2416248Certificate of AnalysisMay 06, 2024 D104213
Propiedades químicas y físicas
SolubilidadInsoluble in water.
Sensibilidadair sensitive
Punto de inflamación (°F)235.4 °F
Punto de inflamación (°C)>110℃
Punto de ebullición (°C)174°C
Punto de fusión (°C)41°C
Peso molecular177.240 g/mol
XLogP32.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count4
Exact Mass177.115 Da
Monoisotopic Mass177.115 Da
Topological Polar Surface Area20.300 Ų
Heavy Atom Count13
Formal Charge0
Complexity146.000
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 Count1
Citations of This Product
Referencias
1. Miaomiao Xing, Yanyan Han, Yilin Zhu, Yatong Sun, Yanyan Shan, Kang-Nan Wang, Qiuxin Liu, Baoli Dong, Duxia Cao, Weiying Lin.  (2022)  Two Ratiometric Fluorescent Probes Based on the Hydroxyl Coumarin Chalcone Unit with Large Fluorescent Peak Shift for the Detection of Hydrazine in Living Cells.  ANALYTICAL CHEMISTRY,      [PMID:36062507] [10.1021/acs.analchem.2c02798]
2. Songsong Tang, Chuanxiang Qin, Hui Li, Guoqiang Chen.  (2019)  Simulation, synthesis, characterisation and dyeing properties of a fluorescent hemicyanine dye.  COLORATION TECHNOLOGY,  136  (1): (23-33).  [PMID:] [10.1111/cote.12432]
3. Jingwen Wang, Min Zheng, Zhigang Xie.  (2018)  Carrier-free core–shell nanodrugs for synergistic two-photon photodynamic therapy of cervical cancer.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:30286310] [10.1016/j.jcis.2018.09.095]
4. Liuheng Wang, Yishi Wu, Yuxia Zhao.  (2017)  Contribution of excited state absorption to optical limiting properties in multi-branched structures.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2017.09.026]
5. Chunlei Yang, Xiu Wang, Haiyun Liu, Shenguang Ge, Mei Yan, Jinghua Yu, Xianrang Song.  (2017)  An inner filter effect fluorescent sensor based on g-C3N4 nanosheets/chromogenic probe for simple detection of glutathione.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2017.04.056]
6. Qianqian Wu, Zian Wang, Jiale Li, Shuang Qiu, Duxia Cao, Zhiqiang Liu, Ruifang Guan.  (2016)  3-Hydroxyflavone derivatives synthesized by a new simple method as chemosensors for cyanide anions.  RSC Advances,  (76): (72698-72702).  [PMID:] [10.1039/C6RA11415F]
7. Yanyan Shan, Zhiqiang Liu, Duxia Cao, Guoqun Liu, Ruifang Guan, Ning Sun, Cong Wang, Kangnan Wang.  (2015)  Coumarinic chalcone derivatives as chemosensors for cyanide anions and copper ions.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2015.06.118]
8. Chun-Yu Zhang, Jing-Hui He, Cai-Jian Lu, Qian-Feng Gu, Lin-Xin Wu, Quan Liu, Hua Li, Qing-Feng Xu, Jian-Mei Lu.  (2015)  Changing the stability of polymer-based memory devices in high conductivity state via tuning the red-ox property of Hemin.  POLYMER,      [PMID:] [10.1016/j.polymer.2015.06.023]
9. Li Yanxia, Liu Zengchen, Zhu Wenping, Fu Hao, Ding Yongjie, Xie Jianping, Yang Weijie, Li Lili, Cheng Chao.  (2015)  Two Different Emission-Wavelength Fluorescent Probes for Aluminum Ion based on Tunable Fluorophores in Aqueous Media.  JOURNAL OF FLUORESCENCE,  25  (3): (603-611).  [PMID:25783983] [10.1007/s10895-015-1541-1]
10. Juan Liu, Peiyang Gu, Feng Zhou, Qingfeng Xu, Jianmei Lu, Hua Li, Lihua Wang.  (2013)  Preparation of TCPP: block copolymer composites and study of their memory behavior by tuning the loading ratio of TCPP in the polymer matrix.  Journal of Materials Chemistry C,  (25): (3947-3954).  [PMID:] [10.1039/C3TC30359D]
11. Azhu Wang, Xianwei Zhao, Zhiwei Shi, Chunyu Lv, Pei Li, Jun Yu, Han Rao, Haining Chen, Huicong Liu, Weiping Li, Xiaoyu Jiang.  (2024)  Developing high-efficiency photoinitiation systems by Leveraging highly Matched Interplays between photosensitizer and photoinitiator for enhanced energy transfer.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2024.113669]
12. Ting Xu, Xiaoting Yan, Ayue Kang, Longhua Yang, Xinhui Li, Yue Tian, Ruige Yang, Shangshang Qin, Yong Guo.  (2024)  Development of Membrane-Targeting Fluorescent 2-Phenyl-1H-phenanthro[9,10-d]imidazole-Antimicrobial Peptide Mimic Conjugates against Methicillin-Resistant Staphylococcus aureus.  JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:38491982] [10.1021/acs.jmedchem.4c00436]
13. Qi Guan, Pei Zeng, Qianqian Zhang, Lili Yu, Guoqiang Wu, Yanping Hong, Chunrong Wang.  (2024)  Highly sensitive detection of tryptophan based on Schiff base reaction and surface-enhanced Raman spectroscopy.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38341934] [10.1016/j.saa.2024.123995]
14. Taiyi Chen, Xiaoping Lin, Peisong Li, Wei Liu, Lu Jiang, Leyuan Huang, Zhongliang Li, Ruirui Zhu, Zhi-Liang Chen, Rongying Zeng, Mengqin Liu, Wen Chen.  (2025)  J-aggregate fluorescence probe constructed based on AIE units for analysis of Zn2+, Cu2+ ions in food and biological systems.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40945013] [10.1016/j.saa.2025.126921]
15. Tian Xinyuan, Bai Xiaoping, Han Yunqi, Ye Yu, Peng Meiling, Cui Hongwei, Li Kai.  (2025)  PPAR γ changing ALDH1A3 content to regulate lipid metabolism and inhibit lung cancer cell growth.  MOLECULAR GENETICS AND GENOMICS,  300  (1): (1-16).  [PMID:40198404] [10.1007/s00438-025-02243-9]
16. Li Hao, Ju Shuguang, Wang Jiacheng, Kuang Donglin, Chen Pengfei, Zhang Mengfan, Qian Ruijie, Liang Chao, Han Daqian, Duan Xuhua.  (2025)  Tanshinone IIA inhibits heat-induced growth of p53-mutant Huh-7 hepatocellular carcinoma by modulating osmotic homeostasis and glycolysis through targeting ALDH7A1.  Cell Death Discovery,  11  (1): (1-20).  [PMID:41173836] [10.1038/s41420-025-02795-0]
17. Wang Pan, Zhang Mengxue, Cai Jun, Chen Zhixuan.  (2026)  Structure and optical properties of polypyrrole oligomers prepared by solution polycondensation.  CHEMICAL PAPERS,      [PMID:] [10.1007/s11696-025-04634-z]
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