2,6-DIMETHYLANILINE HYDROCHLORIDE
- Product Name
- 2,6-DIMETHYLANILINE HYDROCHLORIDE
- CAS No.
- 21436-98-6
- Chemical Name
- 2,6-DIMETHYLANILINE HYDROCHLORIDE
- Synonyms
- Einecs 244-388-1;CompoundAR0033QU;ROPIVACAINE RC A;Compound AR0033QU;Lidocaine Impurity 50;Ropivacaine Impurity A;2,6-DimethylanilineHCl;2,6-xylidinium chloride;Bupivacaine EP Impurity F;2,6-XYLIDINE HYDROCHLORIDE
- CBNumber
- CB6299479
- Molecular Formula
- C8H12ClN
- Formula Weight
- 157.64
- MOL File
- 21436-98-6.mol
2,6-DIMETHYLANILINE HYDROCHLORIDE Property
- Melting point:
- 275°C
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly, Sonicated)
- form
- powder or crystals
- color
- White to Pale Brown
- Stability:
- Hygroscopic
Safety
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- RTECS
- ZF0375000
- HS Code
- 2921490002
- Toxicity
- rat,LD50,oral,2042mg/kg (2042mg/kg),Journal of Pharmacology and Experimental Therapeutics. Vol. 167, Pg. 223, 1969.
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 901252
- Product name
- 2,6-Dimethylaniline hydrochloride
- Purity
- ≥98%
- Packaging
- 1G
- Price
- $44.2
- Updated
- 2025/07/31
- Product number
- PHR2572
- Product name
- Ropivacaine Related Compound A
- Purity
- certified reference material, pharmaceutical secondary standard
- Packaging
- 50MG
- Price
- $557
- Updated
- 2025/07/31
- Product number
- 901252
- Product name
- 2,6-Dimethylaniline hydrochloride
- Purity
- ≥98%
- Packaging
- 5G
- Price
- $121
- Updated
- 2025/07/31
- Product number
- 1605512
- Product name
- Ropivacaine Related Compound A
- Purity
- United States Pharmacopeia (USP) Reference Standard
- Packaging
- 25mg
- Price
- $1470
- Updated
- 2025/07/31
- Product number
- X0029
- Product name
- 2,6-Dimethylaniline Hydrochloride
- Purity
- >98.0%(HPLC)(N)
- Packaging
- 25g
- Price
- $172
- Updated
- 2025/07/31
2,6-DIMETHYLANILINE HYDROCHLORIDE Chemical Properties,Usage,Production
Uses
2,6-Dimethylaniline hydrochloride may be used in the preparation of 2,6-dimethylphenyl isocyanate via phosgenation. This product was previously listed as CDS000447.
Synthesis
2198-53-0
925-90-6
21436-98-6
The general procedure for the synthesis of 2,6-dimethylaniline hydrochloride from 2,6-dimethylacetanilide and ethylmagnesium bromide was as follows: trifluoromethanesulfonic anhydride (Tf2O, 185 μL, 1.1 mmol) was added slowly and dropwise to a cooled-to-0°C dichloromethane ( 4 mL) solution. The reaction mixture was stirred at 0 °C for 30 min, then transferred to -78 °C and a solution of tetrahydrofuran (THF, 15 mL) of freshly prepared organocerium reagent/complex (3.0 mmol) was added, and stirring was continued for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of a 3 mol/L aqueous hydrochloric acid solution (5 mL) and the mixture was gradually warmed to room temperature with continued stirring for 2 hours. Subsequently, 25% ammonium hydroxide solution (5 mL) was added to the mixture. The organic layer was separated and the aqueous phase was extracted with ether (3 x 10 mL). The organic layers were combined, washed with saturated saline (3 x 3 mL) and concentrated under reduced pressure to about 1/3 of the original volume. the residual organic phase was extracted with 3 mol/L aqueous hydrochloric acid solution (3 x 5 mL). The separated organic phase was washed with saturated saline (5 mL), dried with anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure, and the residue was purified by silica gel fast column chromatography to obtain the target ketone product. All aqueous phases were combined, washed with ether (5 mL) and alkalized with 25% ammonium hydroxide solution (5 mL), then back-extracted with ether (5×20 mL). The ether layers were combined, washed with saturated saline (5 mL), dried over anhydrous magnesium sulfate (MgSO4), filtered and acidified with 3 mol/L ethyl acetate hydrochloride solution (5 mL), and finally concentrated under reduced pressure to give 2,6-dimethylaniline hydrochloride.
References
[1] Chinese Chemical Letters, 2015, vol. 26, # 9, p. 1055 - 1058
2,6-DIMETHYLANILINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2,6-DIMETHYLANILINE HYDROCHLORIDE manufacturers
- Product
- Ropivacaine EP Impurity H(Hydrochloride) 21436-98-6
- Price
- US $0.00-0.00/mg
- Min. Order
- 10mg
- Purity
- 99%+ HPLC
- Supply Ability
- 1000
- Release date
- 2025-07-02
- Product
- 2,6-Dimethylaniline Hydrochloride 21436-98-6
- Price
- US $1.00/g
- Min. Order
- 1g
- Purity
- 0.98
- Supply Ability
- 1000
- Release date
- 2024-07-18
- Product
- 2,6-DIMETHYLANILINE HYDROCHLORIDE 21436-98-6
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 10 tons
- Release date
- 2020-01-10