p-Chlorobenzaldehyde - ≥98% , CAS No.104-88-1

CAS: 104-88-1 Cat. No.: C104155 Summenformel: C7H5OCl Molekulargewicht: 140.57 Beilstein Registry Number: 385858 EG-Nummer: 203-247-4
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GRADE & PURITY ≥98%
Synonyms
PCAD | W-108802 | 4-Chlorbenzaldehyd | MFCD00003379 | D77694 | 4-Chlorobenzaldehyd | 4-Chlorobenzaldehyde | 4-chloro-benzaldehyde | 4-formylchlorobenzene | STR00145 | CHLOROBENZALDEHYDE, 4- | EC 203-247-4 | AI3-52280 | bmse001029 | p-Chlorobenzenecarboxal
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
25g
C104155-25g
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8 Auf Lager
9,46€
100g
C104155-100g
—
3 Auf Lager

21,61€

22,47€
Speichern 0,87 € (3.86%)
500g
C104155-500g
1 Auf Lager
3 Auf Lager
43,30€
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Why this grade

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

🌡

Storage & shipping

Room temperature,Argon charged 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.

📚

Literature proof

Cited in 28 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

4-Chlorobenzaldehyde reacts with 3-tert-butyl-N-4-chlorobenzyl-1-phenyl-1H-pyrazol-5-amine to form (E)-3-tert-Butyl-4-(4-chlorobenzyl)-N-(4-chlorobenzylidene)-1-phenyl-1H-pyrazol-5-amine by a microwave-mediated reaction.

Specifications

Synonyme
PCAD | W-108802 | 4-Chlorbenzaldehyd | MFCD00003379 | D77694 | 4-Chlorobenzaldehyd | 4-Chlorobenzaldehyde | 4-chloro-benzaldehyde | 4-formylchlorobenzene | STR00145 | CHLOROBENZALDEHYDE, 4- | EC 203-247-4 | AI3-52280 | bmse001029 | p-Chlorobenzenecarboxal
Spezifikationen & Reinheit
≥98%
Storage
Room temperature,Argon charged
Verschickt in
Normal
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid488180542
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180542
Kanonisches LächelnC1=CC(=CC=C1C=O)Cl
IUPAC Name4-chlorobenzaldehyde
InChIKeyAVPYQKSLYISFPO-UHFFFAOYSA-N
INCHI1S/C7H5ClO/c8-7-3-1-6(5-9)2-4-7/h1-5H
Isomere SMILES C1=CC(=CC=C1C=O)Cl
WGK Deutschland 2
RTECS CU5076000
UN-Nummer 2811
Verpackungsgruppe I
Molekulargewicht 140.57
Beilstein 385858
Reaxy-Rn 385858
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=385858&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
KlasseBenzene and substituted derivatives
SubclassBenzoyl derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoyl derivatives
Alternative Parents Benzaldehydes  Chlorobenzenes  Aryl chlorides  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzoyl - Benzaldehyde - Aryl-aldehyde - Halobenzene - Chlorobenzene - Aryl halide - Aryl chloride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aldehyde - Aromatic homomonocyclic compound
BeschreibungThis 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 monochlorobenzenes - benzaldehydes
3D-Struktur
Interaktives chemisches Strukturmodell





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Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

20 results found

Lot NumberCertificate TypeDatumArtikel
K2217393Certificate of AnalysisSep 22, 2026 C104155
H2631490Certificate of AnalysisAug 19, 2026 C104155
H2631492Certificate of AnalysisAug 19, 2026 C104155
H2631493Certificate of AnalysisAug 19, 2026 C104155
G2629046Certificate of AnalysisOct 24, 2025 C104155
K2510271Certificate of AnalysisOct 24, 2025 C104155
K2510270Certificate of AnalysisOct 24, 2025 C104155
K2510264Certificate of AnalysisOct 24, 2025 C104155
F2101156Certificate of AnalysisDec 18, 2024 C104155
F2101160Certificate of AnalysisDec 18, 2024 C104155
C2414231Certificate of AnalysisMar 02, 2024 C104155
D2409002Certificate of AnalysisFeb 22, 2024 C104155
D2409003Certificate of AnalysisFeb 22, 2024 C104155
F2101155Certificate of AnalysisMar 10, 2023 C104155
L2028019Certificate of AnalysisOct 18, 2022 C104155
K2217397Certificate of AnalysisAug 15, 2022 C104155
K2217396Certificate of AnalysisAug 15, 2022 C104155
K2217395Certificate of AnalysisAug 15, 2022 C104155
K2217394Certificate of AnalysisAug 15, 2022 C104155
K2217392Certificate of AnalysisAug 15, 2022 C104155

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Chemische und physikalische Eigenschaften
LöslichkeitSoluble in water (0.94g/L).
EmpfindlichkeitMoisture sensitive;Light and air Sensitive
Brechungsindex1.5552
Flammpunkt (°F)188.6 °F
Flammpunkt (°C) 87℃
Siedepunkt (°C)213-214°C
Schmelzpunkt (°C)47.5°C
Molekulargewicht140.560 g/mol
XLogP32.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass140.003 Da
Monoisotopic Mass140.003 Da
Topological Polar Surface Area17.100 Ų
Heavy Atom Count9
Formal Charge0
Complexity95.100
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
FAQs und Artikel
Citations of This Product
Referenzen
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4. Siyuan Chang, Sen Zhang, Tianyi Chen, Lei Xu, Sumin Ge, Bingfeng Li, Chenke Yun, Guoxin Zhang, Xuejun He, Xin Pan.  (2023)  Efficient synthesis of 5-hydroxymethyl-2-furancarboxylic acid from bio-based high-concentration 5-hydroxymethylfurfural via highly tolerant aldehyde dehydrogenase.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2023.112966]
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9. Jiuli Han, Lu Bai, Shuangjiang Luo, Bingbing Yang, Yinge Bai, Shaojuan Zeng, Xiangping Zhang.  (2020)  Ionic liquid cobalt complex as O2 carrier in the PIM-1 membrane for O2/N2 separation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2020.117041]
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11. Zhou Liu, Tiyun Yang, Yuxing Huang, Yang Liu, Liucheng Chen, Libo Deng, Ho Cheung Shum, Tiantian Kong.  (2019)  Electrocontrolled Liquid Marbles for Rapid Miniaturized Organic Reactions.  ADVANCED FUNCTIONAL MATERIALS,  29  (19): (1901101).  [PMID:] [10.1002/adfm.201901101]
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13. Yi Huang, Chunyan Wu, Wenwen Yuan, Yongmei Xia, Xiang Liu, Huamei Yang, Haijun Wang.  (2017)  Catalytic Aerobic Oxidation of Biomass-based Furfural into Maleic Acid in Aqueous Phase with Metalloporphyrin Catalysts.  JOURNAL OF THE CHINESE CHEMICAL SOCIETY,  64  (7): (786-794).  [PMID:] [10.1002/jccs.201700004]
14. Wang Qingming, Sun Huifang, Sha Weilin, Chen Juan, Gu Liuyue, Wang Dong, Tang Xinhui.  (2017)  An optical material for the detection of trace S2O3 2− in milk based on a copper complex.  BIOMETALS,  30  (3): (441-447).  [PMID:28405829] [10.1007/s10534-017-0017-y]
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16. Xiuquan Jia, Jiping Ma, Min Wang, Xiaofang Li, Jin Gao, Jie Xu.  (2016)  Alkali α-MnO2/NaxMnO2 collaboratively catalyzed ammoxidation–Pinner tandem reaction of aldehydes.  Catalysis Science & Technology,  6  (20): (7429-7436).  [PMID:] [10.1039/C6CY00874G]
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