4-(2-Chloroethyl)morpholine hydrochloride
- Product Name
- 4-(2-Chloroethyl)morpholine hydrochloride
- CAS No.
- 3647-69-6
- Chemical Name
- 4-(2-Chloroethyl)morpholine hydrochloride
- Synonyms
- MOC;Morpholine, 4-(2-chloroethyl)-, hydrochloride;MOCPRF;4-(2-ChL;ine hydrochL;Chloroethyl Morpholine HCI;Vortioxetine Impurity 70 HCl;2-ChloroethylmorpholineHcl98%;Vortioxetine Impurity 69 DiHCl;N-(2-Chloroethyl)morpholine HCl
- CBNumber
- CB4146399
- Molecular Formula
- C6H13Cl2NO
- Formula Weight
- 186.08
- MOL File
- 3647-69-6.mol
4-(2-Chloroethyl)morpholine hydrochloride Property
- Melting point:
- 180-185 °C (dec.)(lit.)
- storage temp.
- Store below +30°C.
- solubility
- Chloroform (Slightly, Heated), Methanol (Slightly), Water (Slightly)
- form
- Hygroscopic Crystalline Powder
- color
- White to beige
- PH
- 4.5-5 (10g/l, H2O, 20℃)
- Water Solubility
- soluble
- Sensitive
- Hygroscopic
- BRN
- 3684083
- InChI
- InChI=1S/C6H12ClNO.ClH/c7-1-2-8-3-5-9-6-4-8;/h1-6H2;1H
- InChIKey
- NBJHDLKSWUDGJG-UHFFFAOYSA-N
- SMILES
- C1OCCN(CCCl)C1.[H]Cl
- CAS DataBase Reference
- 3647-69-6(CAS DataBase Reference)
- EPA Substance Registry System
- Morpholine, 4-(2-chloroethyl)-, hydrochloride (3647-69-6)
Safety
- Hazard Codes
- T
- Risk Statements
- 21-25-34-43-52/53
- Safety Statements
- 26-36/37/39-45-61
- RIDADR
- UN 2923 8/PG 3
- WGK Germany
- 2
- RTECS
- QE0260000
- Autoignition Temperature
- 365 °C
- TSCA
- Yes
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 29349990
- Toxicity
- LD50 orally in Rabbit: 96 mg/kg LD50 dermal Rat 1502 mg/kg
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H301Toxic if swalloed
H312Harmful in contact with skin
H314Causes severe skin burns and eye damage
H317May cause an allergic skin reaction
H412Harmful to aquatic life with long lasting effects
- Precautionary statements
-
P260Do not breathe dust/fume/gas/mist/vapours/spray.
P273Avoid release to the environment.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
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
- 8.41417
- Product name
- N-(2-Chloroethyl)-morpholinium chloride
- Purity
- for synthesis
- Packaging
- 100g
- Price
- $58
- Updated
- 2025/07/31
- Product number
- 8.41417
- Product name
- N-(2-Chloroethyl)-morpholinium chloride
- Purity
- for synthesis
- Packaging
- 10Kg
- Price
- $1830
- Updated
- 2025/07/31
- Product number
- C42203
- Product name
- 4-(2-Chloroethyl)morpholine hydrochloride
- Purity
- 99%
- Packaging
- 5G
- Price
- $32.3
- Updated
- 2023/06/20
- Product number
- 23051
- Product name
- 4-(2-Chloroethyl)morpholine hydrochloride
- Purity
- purum, ≥97.0% (AT)
- Packaging
- 100g
- Price
- $50
- Updated
- 2023/06/20
- Product number
- C1106
- Product name
- 4-(2-Chloroethyl)morpholine Hydrochloride
- Purity
- >97.0%(T)
- Packaging
- 25g
- Price
- $100
- Updated
- 2025/07/31
4-(2-Chloroethyl)morpholine hydrochloride Chemical Properties,Usage,Production
Chemical Properties
White to beige crystalline powder
Uses
4-(2-Chloroethyl)morpholine hydrochloride (MOC) is used as intermediate for the synthesis of pharmaceuticals (e.g. floredil, morinamide, nimorazole and pholcodine). It is also used as Agrochemical Intermediates, dyestuff Intermediates.
Uses
4-(2-Chloroethyl)morpholine is used in the preparation of potential DNA cross-linking antitumor agents as well as synthetic opiate analogues. 4-(2-Chloroethyl)morpholine may possess sickle-cell hemogl obin aggregation inhibiting-activity.
Safety Profile
Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx.
Synthesis
110-91-8
107-07-3
3647-69-6
General procedure for the synthesis of N-(2-chloroethyl)morpholine hydrochloride from morpholine and 2-chloroethanol: 5.0 mL of morpholine (57.5 mmol) and 4.6 mL of 2-chloroethanol (69.0 mmol) were added to 40 mL of toluene, and heated and refluxed for 2 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and then 8.4 mL (114 mmol) of thionyl chloride was added slowly dropwise under ice bath conditions. After the dropwise addition, the reaction was continued in the ice bath for 20 min, after which the ice bath was removed and the reaction mixture was allowed to stir for 6 h at room temperature. At the end of the reaction, toluene and unreacted thionyl chloride were removed by distillation under reduced pressure. The resulting residue was recrystallized from ethanol to give 7.9 g of N-(2-chloroethyl)morpholine hydrochloride.
References
[1] Patent: US2013/85140, 2013, A1. Location in patent: Paragraph 0074; 0075
[2] Patent: CN104710394, 2017, B. Location in patent: Paragraph 0039-0041
4-(2-Chloroethyl)morpholine hydrochloride Preparation Products And Raw materials
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View Lastest Price from 4-(2-Chloroethyl)morpholine hydrochloride manufacturers
- Product
- 4-(2-Chloroethyl)morpholine hydrochloride 3647-69-6
- Price
- US $242.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 1T
- Release date
- 2021-06-02
- Product
- 4-(2-Chloroethyl)morpholine hydrochloride 3647-69-6
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 20t
- Release date
- 2024-07-15
- Product
- 4- (2-Chloroethyl) Morphol Ine Hydrochloride 3647-69-6
- Price
- US $30.00/G
- Min. Order
- 100G
- Purity
- 99.9%
- Supply Ability
- 5000tons
- Release date
- 2023-07-31