Structure of Propioin
CAS No.: 4984-85-4
*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
4.5
*For Research Use Only! Not for Human Use. We Do Not Sell to Patients.
Change View
| Size | Price | VIP Price |
DE Stock US Stock |
Asia Stock Global Stock |
In Stock |
| {[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} |
Inquiry
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.discount_usd) ]} {[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]} |
Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]} | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_usastock ]} In Stock Inquiry - | {[ item.p_spot_brand_remark ]} 1-2 weeks {[ item.pr_chinastock ]} {[ item.pr_remark ]} In Stock Inquiry - | Login - + |
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ item.p_spot_brand_remark ]}
1-2weeks
Inquiry
Inquiry
{[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price, item.vip_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price, item.pr_usd) ]}
In Stock
- +
Please Login or Create an Account to: See VIP prices and availability
Asia Stock: Ship in 3-5 business days
EU Stock: ship in 0-1 business day
Global Stock: ship in 7-10 days
US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
| CAS No. : | 4984-85-4 |
| Formula : | C6H12O2 |
| M.W : | 116.16 |
| SMILES Code : | OC(C(CC)=O)CC |
| English Name : | 4-Hydroxyhexan-3-one |
| MDL No. : | MFCD00043572 |
| InChI Key : | SKCYVGUCBRYGTE-UHFFFAOYSA-N |
| Pubchem ID : | 95609 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 96.2% | With water; ozone; acetic acid at 5℃; Green chemistry; | 1-3 Embodiment 1 Embodiment 1 A step of 4-hydroxy-3-hexanone oxidation in a synthesis method of 3,4-hexanedione in the invention: first, 116.2 g of 4-hydroxy-3-hexanone (1 mol) and 41 g of water (2.5 mol) are added into a 500 mL three-necked flask for mixing, and then 1.5 g of acetic acid (0.025 mol) used as a cocatalyst is added into the three-necked flask; the three-necked flask is placed in a water bath pot for mixing and stirring by keeping at 5° C.; ozone is introduced into a mixture to carry out an oxidation reaction, a flow rate of the ozone is maintained at 0.3 L/min, and gas chromatography is used for tracking a reaction progress; after the reaction is completed, sodium bisulfite is added into a reaction system to remove ozone remaining in a solution (the ozone remaining in the solution is removed, and otherwise, residual ozone can continue to react to produce by-products during heating in a subsequent distillation process); finally distillation under reduced pressure for separation is carried out to obtain the finished product (3,4-hexanedione). With calculation of 4-hydroxy-3-hexanone, the yield of 3,4-hexanedione is 96.2% in the whole process. Products obtained in the embodiment 1 include: 1H NMR (400 MHz, CDCl3): δ 2.78 (4H, q, 2-CH2-); 1.11 (6H, t, 2-CH3). |
| 86% | With sodium bromide In dichloromethane; water Ambient temperature; anodic oxidation; | |
| 82% | With pyridine; N-Bromosuccinimide In tetrachloromethane for 1.5h; |
| With selenium(IV) oxide | ||
| With copper diacetate; acetic acid | ||
| With water; iron(III) chloride | ||
| With nitric acid | ||
| With aluminum oxide; pumice stone at 320℃; | ||
| With Na<Sb(OAc)6> In 1,4-dioxane Heating; | ||
| With hydroxide at 22.85℃; Photolysis; | ||
| 20 %Chromat. | With oxygen; calcium oxide at 130℃; for 3h; |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With thionyl chloride; <i>N</i>,<i>N</i>-dimethyl-aniline | ||
| With pyridine; thionyl chloride |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With sodium racemat; | ||
| With sodium |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 56% | With sodium In diethyl ether Heating; | |
| 34% | With Na on NaCl support In tetrahydrofuran at 45℃; for 1.5h; | |
| With diethyl ether; sodium man zerlegt die entstandene Natriumverbindung mit Wasser; |
| With sodium; benzene man zerlegt die entstandene Natriumverbindung mit Wasser; | ||
| With sodium | ||
| With sodium In diethyl ether | ||
| With sulfuric acid; sodium 1.) Et2O, xylene, reflux, 2.) Et2O, xylene; Multistep reaction; |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 75% | In benzene for 4h; Heating; | |
| 54% | for 0.0833333h; Irradiation; | |
| With acetic acid |
| In ethanol Reflux; | General procedure for the synthesis of 4,5-bis/disubstituted 1H-imidazol-2(3H)-ones (I1-15) General procedure: The compound from step one, 2-hydroxy-1,2-disubstituted ethanone E1-15 (0.01 mol) and urea (0.01 mol) were mixed in ethanol and refluxed for 3-4 h. Then, the reaction mixture was cooled, solid product was isolated by filtration and recrystallized from ethanol. The purity of the compound was established by thin-layer chromatography using toluene and cyclohexane (7:3) as a mobile phase. |

| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| Irradiation; | ||
| With tripotassium phosphate tribasic; Thauera aromatica alcohol dehydrogenase; nicotinamide adenine dinucleotide In aq. buffer Enzymatic reaction; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| With hydrogenchloride In diethyl ether Heating; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 70% | With sulfur tetrafluoride In diethyl ether at 20℃; for 72h; an autoclave; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 78% | With tert.-butylhydroperoxide; tetraethylammonium acetate In water; toluene; acetonitrile at 0℃; for 18h; Yields of byproduct given; | |
| 1: 40% 2: 50% | With tert.-butylhydroperoxide In water; toluene; acetonitrile at 0℃; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 64% | With sodium hydroxide In water; dimethyl sulfoxide |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 57% | With triethylamine In diethyl ether for 0.5h; | |
| With triethylamine In diethyl ether at 0℃; for 5.5h; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 62% | With sodium hydroxide In water; dimethyl sulfoxide |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 25% | With hydrogenchloride In various solvent(s) for 2h; Heating; | |
| 25% | In various solvent(s) for 5h; Heating; |
| Yield | Reaction Conditions | Operation in experiment |
|---|---|---|
| 57.2% | With potassium carbonate |