ChemicalBook >> CAS DataBase List >>2,2,6,6-Tetramethyl-3,5-heptanedione

2,2,6,6-Tetramethyl-3,5-heptanedione

CAS No.
1118-71-4
Chemical Name:
2,2,6,6-Tetramethyl-3,5-heptanedione
Synonyms
TMHD;2,2,6,6-TETRAMETHYLHEPTANE-3,5-DIONE;DIPIVALOYLMETHANE;2,2,6,6-Tetramethyl heptanedione;2,2,6,6-Tetramethyl-3,5-heptadione;butan-1-ol,propan-2-ol,titanium;3,5-Heptanedione, 2,2,6,6-tetramethyl-;dpm-h;5-heptanedione;6-Tetramethyl-3
CBNumber:
CB1373637
Molecular Formula:
C11H20O2
Molecular Weight:
184.28
MDL Number:
MFCD00008848
MOL File:
1118-71-4.mol
MSDS File:
SDS
Last updated:2024-10-28 16:48:35

2,2,6,6-Tetramethyl-3,5-heptanedione Properties

Melting point >400 °C (decomp)
Boiling point 72-73 °C/6 mmHg (lit.)
Density 0.883 g/mL at 25 °C (lit.)
refractive index n20/D 1.459(lit.)
Flash point 153 °F
storage temp. Sealed in dry,Room Temperature
solubility Difficult to mix.
pka 11.60±0.10(Predicted)
form Liquid
color Clear colorless to slightly yellow
Specific Gravity 0.883
BRN 1447269
InChIKey YRAJNWYBUCUFBD-UHFFFAOYSA-N
LogP 2.818 (est)
CAS DataBase Reference 1118-71-4(CAS DataBase Reference)
FDA UNII R8UI909HOY
EPA Substance Registry System 3,5-Heptanedione, 2,2,6,6-tetramethyl- (1118-71-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H227-H302
Precautionary statements  P210e-P264-P280a-P301+P312a-P501a-P210-P280-P370+P378-P403+P235-P501
Hazard Codes  Xn
Risk Statements  22-40-36/37/38
Safety Statements  24/25-36-26-22
RIDADR  UN 1993 / PGIII
WGK Germany  3
TSCA  T
HS Code  29141900
NFPA 704
2
1 0

2,2,6,6-Tetramethyl-3,5-heptanedione price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 155756 2,2,6,6-Tetramethyl-3,5-heptanedione 98% 1118-71-4 5g $49.8 2024-03-01 Buy
Sigma-Aldrich 155756 2,2,6,6-Tetramethyl-3,5-heptanedione 98% 1118-71-4 25g $144 2024-03-01 Buy
TCI Chemical D1678 Dipivaloylmethane >97.0%(GC) 1118-71-4 5g $61 2024-03-01 Buy
TCI Chemical D1678 Dipivaloylmethane >97.0%(GC) 1118-71-4 25g $173 2024-03-01 Buy
Alfa Aesar A15118 2,2,6,6-Tetramethyl-3,5-heptanedione, 98% 1118-71-4 5g $44.65 2024-03-01 Buy
Product number Packaging Price Buy
155756 5g $49.8 Buy
155756 25g $144 Buy
D1678 5g $61 Buy
D1678 25g $173 Buy
A15118 5g $44.65 Buy

2,2,6,6-Tetramethyl-3,5-heptanedione Chemical Properties,Uses,Production

Chemical Properties

CLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID

Uses

suzuki reaction

Uses

2,2,6,6-Tetramethyl-3,5-heptanedione is a beta diketone with antibacterial activity.

Uses

2,2,6,6-tetramethyl-3,5-heptanedione was used in the synthesis of α-aryl-β-diketones1 and dicyanamidobenzene-bridge diruthenium complex.

Definition

2,2,6,6-Tetramethyl-3,5-heptanedioneis a stable, anhydrous reagent. It undergoes O-additions and C-additions. In various reactions, it acts as an air-stable ligand for metal catalysts. Furthermore, it serves as a substrate for heterocycles.

Synthesis Reference(s)

Journal of the American Chemical Society, 100, p. 5428, 1978 DOI: 10.1021/ja00485a030

General Description

Acylation, a replacement to silylation, allows the conversion of compounds that consist of active hydrogens (-OH, -SH and -NH) into esters, thioesters, and amides via the action of a carboxylic acid or derivative. The carbonyl group adjacent to the halogenated carbons is known to improve the electron capture detector (ECD) response. Acylation has several advantages:

  • It enhances the stability of compounds by protecting unstable groups.
  • It may confer volatility on substances like carbohydrates or amino acids, that have several polar groups that they are non-volatile and usually decompose on heating.
  • It facilitates the separations not possible with underivatized compounds.
  • Compounds are detectable at very low levels with an ECD.

2,2,6,6-Tetramethyl-3,5-heptanedione is a reagent used to form fragmentation-directing derivatives for GC/MS analysis.

Synthesis

Methyl pivalate and formamide could be used as starting materials to synthesize 2,2,6,6-Tetramethyl-3,5-heptanedione.
2,2,6,6-Tetramethyl-3,5-heptanedione   

62688-81-7
1118-71-4
Synthesis of 2,2,6,6-Tetramethyl-3,5-heptanedione from 4-Heptyn-3-one, 2,2,6,6-tetramethyl-
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View Lastest Price from 2,2,6,6-Tetramethyl-3,5-heptanedione manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE pictures 2024-11-22 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE
1118-71-4
US $0.00 / KG 1KG ≥98% HPLC 1000KG Changsha Staherb Natural Ingredients Co., Ltd.
2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE pictures 2024-11-22 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE
1118-71-4
US $205.00-195.00 / KG 25KG 98% 500kg Speranza Chemical Co., Ltd.
2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE pictures 2024-10-28 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE
1118-71-4
US $0.00-0.00 / KG 1KG 99% 500000kg Hebei Weibang Biotechnology Co., Ltd
(CH3)3CCOCH2COC(CH3)3 2,2,6,6-tetramethyl-5-heptanedione 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE DIPIVALOYLMETHANE 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE Dipivaloylmethane~Dpm-H~Tmhd-H 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE, 95 % 2,2,6,6-Tetramethylheptane-3,5-dione,98%TMHD dpm-h 2,2,6,6-TETRAMETHYLHEPTANE-3,5-DIONE TMHD 2,2,6,6-Tetramethyl-3,5-heptanedione, 99+% 2,2,6,6-Tetramethyl-3,5-heptanedione, 98+% 1,3-Di-tert-butyl-1,3-propanedione 2,2,6,6-Tetramethylheptane-3,5-dione, 99% TMHD 2,2,6,6-TetraMethyl-3,5-heptanedione, 98% 5GR 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE FOR 2,2,6,6-TetraMethyl-3,5-heptan Dipivaloylmethane, 3,5-Dioxo-2,2,6,6-tetramethylheptane 2,2,6,6-TetraMethylheptane-3,5-dione SynonyMs 1,3-Di-tert-butyl-1,3-propanedione 2,2,6,6-Tetramethylheptane-3,5-dione 98% 5-heptanedione 6-Tetramethyl-3 Dipivaloylmethane> DIPIVALOYALMETHANE -3,5-heptanedione 2,2,6,6-Tetramethylheptane-3,5-dione 1118-71-4 2,2,6,6-Tetramethyl heptanedione TMHD DIPIVALOYLMETHANE 2,2,6,6-TETRAMETHYLHEPTANE-3,5-DIONE 3,5-Heptanedione, 2,2,6,6-tetramethyl- 2,2,6,6-Tetramethyl-3,5-heptadione butan-1-ol,propan-2-ol,titanium 1118-71-4 11188-71-4 C11H20O2 KETONE Ligands (Environmentally-friendly Oxidation) Environmentally-friendly Oxidation C11 to C12 Carbonyl Compounds Acylation Building Blocks Organic Building Blocks Ketones Achiral Oxygen organic compound Environmentally-friendly Oxidation Ligands (Environmentally-friendly Oxidation) Synthetic Organic Chemistry CHIRAL CHEMICALS