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Merck
CN

D45800

3,5-二叔丁基儿茶酚

98%

别名:

3,5-二叔丁基-1,2-二羟基苯, 3,5-二叔丁基-1,2-苯二醇, 3,5-二叔丁基邻氢醌, 3,5-二叔丁基邻苯二酚, 3,5-双(1,1-二甲基乙基)-1,2-苯二醇, 4,6-二叔丁基-1,2-苯二醇, 4,6-二叔丁基邻苯二酚

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关于此项目

线性分子式:
[(CH3)3C]2C6H2-1,2-(OH)2
化学文摘社编号:
分子量:
222.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-816-9
Beilstein/REAXYS Number:
1370212
MDL number:
Assay:
98%
Form:
crystals
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InChI

1S/C14H22O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8,15-16H,1-6H3

InChI key

PJZLSMMERMMQBJ-UHFFFAOYSA-N

SMILES string

CC(C)(C)c1cc(O)c(O)c(c1)C(C)(C)C

assay

98%

form

crystals

Quality Level

mp

95-100 °C (lit.)

Application

3,5-二-丁基儿茶酚可用作:
  • 通过催化氧化制备3,5-二--丁基醌的反应物。
  • 苯乙烯和丁二烯等单体生产中的聚合抑制剂。
  • 以L-脯氨酸为催化剂通过不对称亚硝基羟醛缩反应合成对映选择性 1,2-恶嗪烷和异恶唑烷的添加剂。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

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Jens Ackermann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(1), 247-258 (2002-02-02)
Dicopper(II) complexes of a series of different pyrazolate-based dinucleating ligands [L1](-)-[L4](-) have been synthesized and characterized structurally and spectroscopically. A major difference between the four complexes is the individual metal-metal separation that is enforced by the chelating side arms of
Christopher Grieco et al.
Nature communications, 11(1), 4569-4569 (2020-09-13)
Eumelanin is a brown-black biological pigment with sunscreen and radical scavenging functions important to numerous organisms. Eumelanin is also a promising redox-active material for energy conversion and storage, but the chemical structures present in this heterogeneous pigment remain unknown, limiting
Vasiliki Lykourinou et al.
Journal of the American Chemical Society, 133(27), 10382-10385 (2011-06-21)
Microperoxidase-11 has for the first time been successfully immobilized into a mesoporous metal-organic framework (MOF) consisting of nanoscopic cages and it demonstrates superior enzymatic catalysis performances compared to its mesoporous silica counterpart.
Michael U Triller et al.
Inorganic chemistry, 42(20), 6274-6283 (2003-09-30)
The manganese compounds [Mn(bpia)(OAc)(OCH(3))](PF(6)) (1), [Mn(bipa)(OAc)(OCH(3))](PF(6)) (2), [Mn(bpia)(Cl)(2)](ClO(4)) (3), [Mn(bipa)(Cl)(2)](ClO(4)) (4), [Mn(Hmimppa)(Cl)(2)] x CH(3)OH (5), and [Mn(mimppa)(TCC)] x 2CHCl(3) (6) (bpia = bis(picolyl)(N-methylimidazole-2-yl)amine; bipa = bis(N-methylimidazole-2-yl)(picolyl)amine; Hmimppa = ((1-methylimidazole-2-yl)methyl)((2-pyridyl)methyl)(2-hydroxyphenyl)amine; TCC = tetrachlorocatechol) were synthesized and characterized by various techniques such
Paramita Kar et al.
Inorganic chemistry, 51(7), 4265-4273 (2012-03-16)
A multifunctional porous metal organic framework based on mixed-valence hexa-nuclear [Mn(III)(2)Mn(II)(4)O(2)(pyz)(2)(C(6)H(5)CH(2)COO)(10)] (pyz = pyrazine) units has been synthesized. The complex has been characterized by elemental analysis, IR spectroscopy, single-crystal X-ray diffraction analysis, and variable-temperature magnetic measurements. The structural analysis reveals

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