2,6-Diisopropylaniline - ≥95% , CAS No.24544-04-5

CAS: 24544-04-5 Cat. No.: D109348 Peso molecular: 177.29 Beilstein Registry Number: 2208763 Número EC: 246-305-4
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
EN300-19395 | 2,6-Diisopropylaniline, 97% | 2,6-Dilsopropylaniline | Q27252049 | 2,6-di(propan-2-yl)aniline | DTXSID5022279 | DIPA 2,6-DIISOPROPYLANILINE 2,6-bis(1-methylethyl)-benzenamin | InChI=1/C12H19N/c1-
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
D109348-25ml
4
10,90US$
100ml
D109348-100ml
5
23,90US$
500ml
D109348-500ml
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
82,90US$
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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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.

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Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

2,6-Diisopropylaniline is an amine. It undergoes condensation with triacetylmethane in toluene in the presence of p-toluenesulfonic acid provides 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione. 2,6-Diisopropylaniline is an aromatic amine. It reacts with bis(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands to afford yttrium alkyl anilido species. This reaction involves the elimination of TMS (Trimethylsilane). Used to prepare N-heterocyclic carbene complexes for α-arylation of acyclic ketones, amination of haloarenes,and aqueous Suzuki coupling.

Specifications

Sinónimos
EN300-19395 | 2, 6-Diisopropylaniline, 97% | 2, 6-Dilsopropylaniline | Q27252049 | 2, 6-di(propan-2-yl)aniline | DTXSID5022279 | DIPA 2, 6-DIISOPROPYLANILINE 2, 6-bis(1-methylethyl)-benzenamin | InChI=1/C12H19N/c1-
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Pureza
≥95%
Nombres e identificadores
Pubchem Sid488183188
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488183188
Sonrisas canónicasCC(C)C1=C(C(=CC=C1)C(C)C)N
IUPAC Name2,6-di(propan-2-yl)aniline
InChIKeyWKBALTUBRZPIPZ-UHFFFAOYSA-N
INCHI1S/C12H19N/c1-8(2)10-6-5-7-11(9(3)4)12(10)13/h5-9H,13H2,1-4H3
Isómeros SMILES CC(C)C1=C(C(=CC=C1)C(C)C)N
WGK Alemania 2
RTECS BX4025000
Peso molecular 177.29
Beilstein 2208763
Reaxy-Rn 2208763
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2208763&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
SubclassCumenes
Intermediate Tree Nodes Not available
Direct ParentCumenes
Alternative Parents Phenylpropanes  Aniline and substituted anilines  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Phenylpropane - Cumene - Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as cumenes. These are aromatic compounds containing a prop-2-ylbenzene moiety.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

16 results found

Lot NumberCertificate TypeFechaArticulo
H2130131Certificate of AnalysisApr 03, 2026 D109348
D2610498Certificate of AnalysisMar 27, 2026 D109348
D2610500Certificate of AnalysisMar 27, 2026 D109348
D2610505Certificate of AnalysisMar 27, 2026 D109348
D2610506Certificate of AnalysisMar 27, 2026 D109348
B2308417Certificate of AnalysisMar 13, 2026 D109348
B2308100Certificate of AnalysisMar 13, 2026 D109348
L1904101Certificate of AnalysisFeb 05, 2026 D109348
L2512093Certificate of AnalysisDec 16, 2025 D109348
B2218424Certificate of AnalysisDec 12, 2025 D109348
B2218427Certificate of AnalysisDec 12, 2025 D109348
B2519034Certificate of AnalysisDec 12, 2025 D109348
D2511474Certificate of AnalysisJun 17, 2024 D109348
D2511410Certificate of AnalysisJun 17, 2024 D109348
B2218441Certificate of AnalysisDec 12, 2022 D109348
H2130132Certificate of AnalysisJun 24, 2022 D109348

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Propiedades químicas y físicas
SolubilidadMiscible with ether and alcohol. Slightly miscible with water.
SensibilidadAir Sensitive
Índice de refracción1.532
Punto de inflamación (°F)242.6 °F
Punto de inflamación (°C)117°C
Punto de ebullición (°C)257°C
Punto de fusión (°C)-45°C
Peso molecular177.290 g/mol
XLogP33.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass177.152 Da
Monoisotopic Mass177.152 Da
Topological Polar Surface Area26.000 Ų
Heavy Atom Count13
Formal Charge0
Complexity135.000
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. Cuicui Wu, Pan Feng, Xuan Guo, Yunming Fang.  (2023)  Purification of artemisinin precursor amorphadiene from microbial metabolites containing isomeride farnesene: Solid-Pd chemocatalysis of farnesene to squalene with high boiling point.  CATALYSIS COMMUNICATIONS,      [PMID:] [10.1016/j.catcom.2023.106770]
2. Pengbo Wang, Qian He, Hao Zhang, Qingdi Sun, Yujie Cheng, Tao Gan, Xiaohui He, Hongbing Ji.  (2020)  N-formylation of amines using phenylsilane and CO2 over ZnO catalyst under mild condition.  CATALYSIS COMMUNICATIONS,      [PMID:] [10.1016/j.catcom.2020.106195]
3. Tianyun Li, Huahua Huang, Lei Wang, Yongming Chen.  (2017)  High performance polyimides with good solubility and optical transparency formed by the introduction of alkyl and naphthalene groups into diamine monomers.  RSC Advances,  (65): (40996-41003).  [PMID:] [10.1039/C7RA07142F]
4. Liu Bo, Liu Dong-tao, Li Shi-hui, Sun Guang-ping, Cui Dong-mei.  (2015)  High trans-1,4 (co)polymerization of β-myrcene and isoprene with an iminophosphonamide lanthanum catalyst.  CHINESE JOURNAL OF POLYMER SCIENCE,  34  (1): (104-110).  [PMID:] [10.1007/s10118-016-1729-0]
5. Limiao Lin, Yonghang Xu, Shuanjin Wang, Min Xiao, Yuezhong Meng.  (2015)  Ring-opening polymerization of l-lactide and ε-caprolactone catalyzed by versatile tri-zinc complex: Synthesis of biodegradable polyester with gradient sequence structure.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2015.09.029]
6. Bo Liu, Guangping Sun, Shihui Li, Dongtao Liu, Dongmei Cui.  (2015)  Isoprene Polymerization with Iminophosphonamide Rare-Earth-Metal Alkyl Complexes: Influence of Metal Size on the Regio- and Stereoselectivity.  ORGANOMETALLICS,      [PMID:] [10.1021/acs.organomet.5b00502]
7. Liu Bo, Han Bao-yu, Zhang Chun-ling, Li Shi-hui, Sun Guang-ping, Cui Dong-mei.  (2015)  Renewable β-myrcene polymerization initiated by lutetium alkyl complexes ligated by imidophosphonamido ligand.  CHINESE JOURNAL OF POLYMER SCIENCE,  33  (5): (792-796).  [PMID:] [10.1007/s10118-015-1629-8]
8. Yonghang Xu, Shuanjin Wang, Limiao Lin, Min Xiao, Yuezhong Meng.  (2014)  Semi-crystalline terpolymers with varying chain sequence structures derived from CO2, cyclohexene oxide and ε-caprolactone: one-step synthesis catalyzed by tri-zinc complexes.  Polymer Chemistry,  (9): (1533-1540).  [PMID:] [10.1039/C4PY01587H]
9. Shuang Chen, Qiule Zhao, Yangchun Mo, Xiaopeng Wei, Jilin Wang, Guoyuan Zheng, Fei Long.  (2025)  Crystal structure, thermal stability and photoelectric performance of the organic-inorganic hybrid material [(CH3CH2CH2)2NH2]aBibXc (X = Cl, Br and I).  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2025.180131]
10. Xuexin Yuan, Qiqi Zhou, Yu Chen, Hai-Jian Yang, Qingqing Jiang, Juncheng Hu, Cun-Yue Guo.  (2024)  Photocatalytic N-Formylation of CO2 with Amines Catalyzed by Diethyltriamine Pentaacetic Acid.  C-Journal of Carbon Research,  10  (3): (62).  [PMID:] [10.3390/c10030062]
11. Hui Niu, Huan Lin, Huiting Zhang, Longfeng Hu, Gangqiang Yu, Shuhong Wu, Jinlin Long, Quan-Fu An.  (2025)  Synergistic bulk and surface electric fields in self-assembled perylene-based nanosheets expedite photocatalytic hydrogen evolution.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2025.125519]
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