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| 112-20-9 Chemical Structure| 112-20-9

Structure of 112-20-9

Chemical Structure| 112-20-9

*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 [ 112-20-9 ]

CAS No. :112-20-9
Formula : C9H21N
M.W : 143.27
SMILES Code : CCCCCCCCCN
MDL No. :MFCD00008249
InChI Key :FJDUDHYHRVPMJZ-UHFFFAOYSA-N
Pubchem ID :16215

Safety of [ 112-20-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302+H312+H332-H314-H400
Precautionary Statements:P273-P280-P305+P351+P338-P310
Class:8
UN#:2735
Packing Group:

Application In Synthesis of [ 112-20-9 ]

* 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 [ 112-20-9 ]

[ 112-20-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 112-20-9 ]
  • [ 546-43-0 ]
  • [ 1245718-97-1 ]
  • 2
  • [ 112-20-9 ]
  • [ 19064-24-5 ]
  • [ 1423875-65-3 ]
YieldReaction ConditionsOperation in experiment
89.5% With potassium carbonate; In N,N-dimethyl acetamide; toluene; at 125℃; for 17h;Dean-Stark; General procedure: The preparation of compound A7 is provided as a representative synthesis procedure of these compounds. (0012) Heptylamine (1.3186 g, 0.0114 mol) and 2,4-DFNB, (0.9262 g, 0.0058 mol) were weighed into separate vials. Potassium carbonate (3.03 g, 0.022 mol, 50% excess) was transferred to a 100 mL three-necked round-bottomed flask fitted with a magnetic stir bar, nitrogen inlet, thermometer, and a Dean-Stark trap fitted with a condenser. Each glass vial used for weighing starting materials was rinsed with DMAC (5 mL) and the washings were transferred to the reaction vessel to ensure full transfer of any residual reagents. Next, an additional 4 mL of DMAC was added to the reaction vessel, followed by 15 mL of toluene. An initial exotherm of 5 C was observed upon the dissolution of the starting materials, rendering the reaction mixture bright yellow in color. The reaction vessel was heated by an external temperature-controlled oil bath (with mild stirring) for 17 h at 125 C. At the completion of the reaction, the vessel was cooled, the reaction mixture was diluted with dichloromethane, and then filtered through celite to remove all salts. The filtrate was evaporated at reduced pressure to yield a crude product that was subsequently dissolved in dichloromethane and washed with water. The organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated at reduced pressure, and the resulting solid was further purified via recrystallization in absolute ethanol to yield yellow needles. Spectroscopic data for the secondary amines are supplied as Supplementary data.
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 112-20-9 ]

Aliphatic Chain Hydrocarbons

Chemical Structure| 14130-06-4

A237222 [14130-06-4]

Docosan-1-amine

Similarity: 1.00

Chemical Structure| 2016-57-1

A412856 [2016-57-1]

Decan-1-amine

Similarity: 1.00

Chemical Structure| 124-30-1

A525938 [124-30-1]

Octadecan-1-amine

Similarity: 1.00

Chemical Structure| 10525-37-8

A884758 [10525-37-8]

Icosan-1-amine

Similarity: 1.00

Chemical Structure| 929-73-7

A412708 [929-73-7]

Dodecan-1-amine hydrochloride

Similarity: 0.91

Amines

Chemical Structure| 14130-06-4

A237222 [14130-06-4]

Docosan-1-amine

Similarity: 1.00

Chemical Structure| 124-30-1

A525938 [124-30-1]

Octadecan-1-amine

Similarity: 1.00

Chemical Structure| 10525-37-8

A884758 [10525-37-8]

Icosan-1-amine

Similarity: 1.00

Chemical Structure| 111-86-4

A132244 [111-86-4]

N-octylamine

Similarity: 1.00

Chemical Structure| 4200-95-7

A868126 [4200-95-7]

1-Aminoheptadecane

Similarity: 1.00