| Identification | Back Directory | [Name]
3-TERT-BUTYLADIPIC ACID | [CAS]
10347-88-3 | [Synonyms]
3-TERT-BUTYLADIPIC A
3-T-BUTYL ADIPIC ACID
3-TERT-BUTYLADIPIC ACID
3-(tert-Butyl)hexanedioic
3-T-BUTYL ADIPIC ACID 99%
3-t-Butyl-hexanedioic acid
3-Tert-butylhexandioicacid
beta-tert-Butyl-adipic acid
3-tert-Butyladipic acid,99%
3-tert-Butylhexanedioic acid
3-tert-Butyl-1,6-hexanedioic acid
3-(1,1-DIMETHYLETHYL)HEXANEDIOIC ACID
DIMETHYLAMINE, 40 WT. % SOLUTION IN WATE R
3-tert-Butyladipic acid3-(1,1-Dimethylethyl)hexanedioic acid | [EINECS(EC#)]
233-759-3 | [Molecular Formula]
C10H18O4 | [MDL Number]
MFCD00020550 | [MOL File]
10347-88-3.mol | [Molecular Weight]
202.25 |
| Chemical Properties | Back Directory | [Appearance]
white fine crystalline powder | [Melting point ]
112-115 °C(lit.)
| [Boiling point ]
375.34°C (rough estimate) | [density ]
1.103 | [vapor pressure ]
0Pa at 20℃ | [refractive index ]
1.4393 (estimate) | [Fp ]
213 °C
| [pka]
4.70±0.10(Predicted) | [Water Solubility ]
4.89g/L at 20℃ | [LogP]
1.59 at 20℃ |
| Hazard Information | Back Directory | [Chemical Properties]
white fine crystalline powder | [Uses]
3-(tert-Butyl)hexanedioic acid is a useful reactant for the synthesis of hexamethylenetetrathiafulvalene derivatives with substituted bulky alkyl groups which are studied for their transistor properties. | [Definition]
ChEBI: 3-tert-butyladipic acid is a medium-chain fatty acid. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 99, p. 4405, 1977 DOI: 10.1021/ja00455a032
Synthesis, p. 915, 1988 DOI: 10.1055/s-1988-27754 | [Flammability and Explosibility]
Notclassified | [Synthesis]
The general procedure for synthesizing 3-tert-butyl adipic acid from p-tert-butylcyclohexanol was as follows: the operating conditions were kept the same as those of Example 2, except that the alicyclic secondary alcohol compounds or alicyclic ketone compounds listed in Table 2 were used instead of cyclohexanol as starting materials. The experimental results are detailed in Table 2. | [References]
[1] Tetrahedron Letters, 2004, vol. 45, # 44, p. 8221 - 8224
[2] Patent: EP1728779, 2006, A1. Location in patent: Page/Page column 6
[3] Patent: US1960211, 1932,
[4] Journal of the American Chemical Society, 1939, vol. 61, p. 2728
[5] Journal of the American Chemical Society, 1951, vol. 73, p. 2540,2542 |
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