Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 16649-50-6 Chemical Structure| 16649-50-6

Structure of 16649-50-6

Chemical Structure| 16649-50-6

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 16649-50-6 ]

CAS No. :16649-50-6
Formula : C4H11NO
M.W : 89.14
SMILES Code : ONC(C)(C)C
MDL No. :MFCD06653532
InChI Key :XWESXZZECGOXDQ-UHFFFAOYSA-N
Pubchem ID :98586

Safety of [ 16649-50-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H228
Precautionary Statements:P210-P273-P243-P403
Class:4.1
UN#:1325
Packing Group:

Application In Synthesis of [ 16649-50-6 ]

* 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.

  • Downstream synthetic route of [ 16649-50-6 ]

[ 16649-50-6 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 16649-50-6 ]
  • [ 82657-74-7 ]
  • C12H19NO3S [ No CAS ]
  • 2
  • [ 16649-50-6 ]
  • [ 56442-17-2 ]
  • [ 223650-14-4 ]
YieldReaction ConditionsOperation in experiment
98.5% toluene-4-sulfonic acid; Example 47 Synthesis of α-[4-(4-Fluorobenzyloxy)phenyl]-N-tert-butylnitrone The title compound was prepared by refluxing a benzene solution of <strong>[56442-17-2]4-(4-fluorobenzyloxy)benzaldehyde</strong> and N-tert-butylhydroxylamine for 21 hours with p-toluenesulfonic acid as a catalyst. The title compound was obtained as a solid in 98.5% yield, m.p. 180.3 C. (Rf =0.16 on a silica gel plate using hexanes: EtOAc, 1:1, v/v, as an eluant).
  • 3
  • [ 16649-50-6 ]
  • [ 186534-02-1 ]
  • [ 1083171-75-8 ]
YieldReaction ConditionsOperation in experiment
38% In methanol;Reflux; Example 1 Synthesis of TBN (FIG. 2) 2-[[(1,1-Dimethylethyl)oxidoimino]methyl]-3,5,6-trimethylpyrazine (TBN). To aldehyde 5 (1.9 g, 0.013 mol) in methanol (200 mL) was added tert-butylhydroxylamine (1 g, 0.011 mol), and the solution was refluxed for 2 h. Another portion of tert-butyl hydroxylamine (1 g, 0.011 mol) was then added, and the solution refluxed until aldehyde 5 was completely reacted. Solvent was removed in vacuo, and the product was extracted. The solution was dried with Na2SO4, and solvent removed in vacuo. The product was purified by column chromatography, eluding with ethyl acetate/petroleum ether (1/1, v/v), to produce TBN as a light yellow solid (1.1 g, 38% yield), mp: 68-70 C. 1H NMR (CDCl3, ppm): 7.82 (s, 1H), 2.47 (s, 3H), 2.50 (s, 3H), 2.52 (s, 3H), 1.63 (s, 9H). ESI-MS: 222 [M+H]+, 244 [M+Na]+. Anal. (C12H19N3O) C, H, N.
38% In mthanol;Reflux; To aldehyde 5 (1.9 g, 0.013 mol) in methanol (200 mL) was added tert-butylhydroxylamine (1 g, 0.011 mol), and the solution was refluxed for 2 h. Another portion of tert-butyl hydroxy lamine (1 g, 0.011 mol) was then added, and the solution refluxed until aldehyde 5 was completely reacted. Solvent was removed in vacuo, and the product was extracted. The solution was dried with Na2SO4, and solvent removed in vacuo. The product was purified by column chromatography, eluting with ethyl acetate/petroleum ether (1/1, v/v), to produce TBN as a light yellow solid (1.1 g, 38% yield), mp: 68-70 0C. 1H NMR (CDCl3, ppm): 7.82 (s, IH), 2.47 (s, 3H), 2.50 (s, 3H), 2.52 (s, 3H), 1.63 (s, 9H). ESI-MS: 222 [M+H]+, 244 [M+Na]+. Anal. (Ci2H19N3O) C, H, N.
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 16649-50-6 ]

Aliphatic Chain Hydrocarbons

Chemical Structure| 57497-39-9

A245257 [57497-39-9]

N-(tert-Butyl) hydroxylamine hydrochloride

Similarity: 0.93

Amines

Chemical Structure| 57497-39-9

A245257 [57497-39-9]

N-(tert-Butyl) hydroxylamine hydrochloride

Similarity: 0.93

Hydroxylamines

Chemical Structure| 57497-39-9

A245257 [57497-39-9]

N-(tert-Butyl) hydroxylamine hydrochloride

Similarity: 0.93