Cas no 3279-07-0 (4-tert-Butyl-2-nitrophenol)
4-tert-Butyl-2-nitrophenol Chemical and Physical Properties
Names and Identifiers
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- 4-(tert-Butyl)-2-nitrophenol
- Phenol, 4-(1,1-dimethylethyl)-2-nitro
- 4-T-BUTYL-2-NITROPHENOL
- 4-TERT-BUTYL-2-NITROPHENOL
- 2-Nitryl-4-tert-butylphenol
- O-NITRO-P-(TERT)BUTYL PHENOL
- 2-NITRO-4-TERT-BUTYLPHENOL
- 3-Nitro-4-hydroxy-1-tert.-butyl-benzol
- 4-(1,1-dimethylethyl)-2-nitro-phenol
- FT-0658448
- AS-14489
- SCHEMBL445240
- B1812
- 4-(t-butyl)-2-nitrophenol
- NSC36629
- 4-tert.-butyl-2-nitrophenol
- 4-t-butyl-2-nitro-phenol
- Phenol, 4-(1,1-dimethylethyl)-2-nitro-
- 4-tert-butyl-2-nitro-phenol;2-Nitro-4-tert-butylphenol
- o-nitro-p-t-butyl-phenol
- 2-nitro-4-t-butyl phenol
- AC-12203
- W-106822
- A821416
- 3279-07-0
- InChI=1/C10H13NO3/c1-10(2,3)7-4-5-9(12)8(6-7)11(13)14/h4-6,12H,1-3H
- 4-tert-Butyl-2-nitrophenol, 97%
- DTXSID9074642
- AKOS005173947
- UNII-Q94NDU9GTF
- NSC 36629
- 2-nitro-4-tert-butyl phenol
- NSC-36629
- NS00029348
- 4-(1,1-DIMETHYLETHYL)-2-NITROPHENOL
- CS-W010626
- MFCD00191888
- EINECS 221-914-8
- Q94NDU9GTF
- ALBB-013847
- DA-06863
- DTXCID2038574
- 4-tert-Butyl-2-nitrophenol
-
- MDL: MFCD00191888
- Inchi: 1S/C10H13NO3/c1-10(2,3)7-4-5-9(12)8(6-7)11(13)14/h4-6,12H,1-3H3
- InChI Key: IHGNADPMUSNTJW-UHFFFAOYSA-N
- SMILES: OC1C=CC(=CC=1[N+](=O)[O-])C(C)(C)C
Computed Properties
- Exact Mass: 195.09000
- Monoisotopic Mass: 195.09
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 216
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 66A^2
- Surface Charge: 0
- Tautomer Count: 4
- XLogP3: nothing
Experimental Properties
- Color/Form: Uncertain
- Density: 1.12?g/mL?at 25?°C(lit.)
- Melting Point: 27-29?°C (lit.)
- Boiling Point: 97?°C/1?mmHg(lit.)
- Flash Point: Degrees Fahrenheit:235.4°F
Degrees Celsius:113°C - Refractive Index: 1.5500-1.5530
- PSA: 66.05000
- LogP: 3.12110
- Solubility: Uncertain
4-tert-Butyl-2-nitrophenol Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H315,H319,H335
- Warning Statement: P261,P305+P351+P338
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26-S36
-
Hazardous Material Identification:
- Risk Phrases:R36/37/38
- HazardClass:IRRITANT
- Storage Condition:Store at room temperature
- Safety Term:S26;S36
4-tert-Butyl-2-nitrophenol Customs Data
- HS CODE:2908999090
- Customs Data:
China Customs Code:
2908999090Overview:
2908999090 Halogenated derivatives of other phenols and phenolic alcohols(Including its sulfonation\Nitrosative or nitrosative derivatives). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2908999090 halogenated, sulphonated, nitrated or nitrosated derivatives of phenols or phenol-alcohols.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:5.5%.General tariff:30.0%
4-tert-Butyl-2-nitrophenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 412600-25G |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 97% | 25G |
¥1382.34 | 2022-02-24 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B1812-25g |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 98.0%(GC) | 25g |
¥910.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B1812-5g |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 98.0%(GC) | 5g |
¥260.0 | 2022-06-10 | |
| Matrix Scientific | 063678-500mg |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 500mg |
$158.00 | 2023-09-10 | ||
| Fluorochem | 226519-1g |
4-(tert-Butyl)-2-nitrophenol |
3279-07-0 | 95% | 1g |
£10.00 | 2022-02-28 | |
| Fluorochem | 226519-5g |
4-(tert-Butyl)-2-nitrophenol |
3279-07-0 | 95% | 5g |
£34.00 | 2022-02-28 | |
| Fluorochem | 226519-25g |
4-(tert-Butyl)-2-nitrophenol |
3279-07-0 | 95% | 25g |
£98.00 | 2022-02-28 | |
| Fluorochem | 226519-100g |
4-(tert-Butyl)-2-nitrophenol |
3279-07-0 | 95% | 100g |
£341.00 | 2022-02-28 | |
| TRC | B810363-2.5g |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 2.5g |
$ 52.00 | 2023-09-08 | ||
| TRC | B810363-5g |
4-tert-Butyl-2-nitrophenol |
3279-07-0 | 5g |
$ 64.00 | 2023-09-08 |
4-tert-Butyl-2-nitrophenol Suppliers
4-tert-Butyl-2-nitrophenol Related Literature
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
-
Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
-
Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
Additional information on 4-tert-Butyl-2-nitrophenol
4-tert-Butyl-2-nitrophenol (CAS 3279-07-0): Properties, Applications, and Market Insights
4-tert-Butyl-2-nitrophenol (CAS 3279-07-0) is a specialized organic compound with significant industrial relevance. This yellow crystalline solid belongs to the class of nitrophenol derivatives, characterized by the presence of both a nitro group (-NO?) and a hydroxyl group (-OH) on an aromatic ring. The tert-butyl substituent at the 4-position enhances its unique chemical properties, making it valuable for various technical applications.
The molecular formula of 4-tert-butyl-2-nitrophenol is C??H??NO?, with a molecular weight of 195.22 g/mol. Its structural features contribute to several interesting characteristics: moderate solubility in organic solvents, thermal stability up to 200°C, and distinct UV-visible absorption properties. These physicochemical properties make it particularly useful in specialty chemical formulations where controlled reactivity is required.
In industrial applications, 4-tert-butyl-2-nitrophenol CAS 3279-07-0 serves multiple functions. It acts as an intermediate in the synthesis of more complex organic compounds, particularly in the production of azo dyes and photostabilizers. The compound's ability to absorb specific wavelengths of light makes it valuable in UV-absorbing materials, a property increasingly sought after in polymer stabilization and coatings technology.
Recent market trends show growing demand for nitrophenol derivatives in sustainable material development. Researchers are exploring the use of 4-tert-butyl-2-nitrophenol in green chemistry applications, particularly as a building block for environmentally friendly photoinitiators. This aligns with current industry focus on eco-friendly chemical solutions and reduced environmental impact manufacturing processes.
The synthesis of 4-tert-butyl-2-nitrophenol typically involves nitration of 4-tert-butylphenol under controlled conditions. Modern production methods emphasize atom economy and waste minimization, reflecting the chemical industry's shift toward sustainable practices. Quality control parameters for commercial material generally specify ≥98% purity, with HPLC analysis becoming the standard verification method.
From a safety perspective, proper handling of 4-tert-butyl-2-nitrophenol requires standard laboratory precautions. While not classified as hazardous under normal conditions, it should be stored in cool, dry environments away from strong oxidizers. These handling considerations are particularly important for formulators working with specialty chemical intermediates in industrial settings.
Analytical characterization of CAS 3279-07-0 typically includes GC-MS, FTIR, and NMR spectroscopy. The compound shows characteristic peaks in these analyses that facilitate quality verification. Recent advances in analytical chemistry techniques have improved detection limits for trace impurities, ensuring higher purity standards for technical applications.
The global market for nitrophenol derivatives shows steady growth, with 4-tert-butyl-2-nitrophenol maintaining a niche position. Asia-Pacific regions demonstrate particularly strong demand, driven by expanding specialty chemicals manufacturing capabilities. Price trends reflect raw material costs and regional production capacities, with technical grade material typically trading in the range of $50-80/kg depending on purity and order volume.
Emerging research directions for 4-tert-butyl-2-nitrophenol include potential applications in organic electronics and advanced material science. Its electron-withdrawing nitro group and aromatic structure make it interesting for molecular engineering of functional materials. These developments align with current scientific interest in tailored organic compounds for next-generation technologies.
For researchers and industrial users seeking 4-tert-butyl-2-nitrophenol suppliers, key selection criteria include consistent quality, reliable supply chains, and comprehensive technical documentation. Many manufacturers now provide custom synthesis services for derivative compounds, responding to the growing need for specialized chemical intermediates in various industries.
Environmental considerations for 4-tert-butyl-2-nitrophenol focus on biodegradation pathways and ecotoxicological profiles. Modern production facilities implement waste treatment protocols to minimize environmental release. These practices address increasing regulatory requirements and industry commitments to sustainable chemical manufacturing principles.
In formulation science, the compatibility of 4-tert-butyl-2-nitrophenol with various matrices is an important consideration. Its performance in polymer systems and coating formulations depends on factors like solubility parameters and thermal stability. These characteristics are particularly relevant for applications requiring long-term material performance.
Looking forward, innovation in nitrophenol chemistry continues to expand the potential uses of 4-tert-butyl-2-nitrophenol. Current research explores its role in catalysis and molecular recognition systems, demonstrating the compound's versatility beyond traditional applications. These developments contribute to the growing importance of functionalized phenols in advanced chemical technologies.
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