ChemicalBook--->CAS DataBase List--->15572-56-2

15572-56-2

15572-56-2 Structure

15572-56-2 Structure
IdentificationMore
[Name]

ISOPROPYLAMINE HYDROCHLORIDE
[CAS]

15572-56-2
[Synonyms]

2-AMINOPROPANE HYDROCHLORIDE
ISOPROPYLAMINE HCL
ISOPROPYLAMINE HYDROCHLORIDE
MONOISOPROPYLAMINE HYDROCHLORIDE
2-propanamine,hydrochloride
isopropylammoniumchloride
Isopropyl-ammoniumchloride
[EINECS(EC#)]

239-629-2
[Molecular Formula]

C3H10ClN
[MDL Number]

MFCD00050705
[Molecular Weight]

95.57
[MOL File]

15572-56-2.mol
Chemical PropertiesBack Directory
[Melting point ]

160°C
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Methanol (Slightly), Water
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
[InChI]

InChI=1S/C3H9N.ClH/c1-3(2)4;/h3H,4H2,1-2H3;1H
[InChIKey]

ISYORFGKSZLPNW-UHFFFAOYSA-N
[SMILES]

C(N)(C)C.Cl
[CAS DataBase Reference]

15572-56-2(CAS DataBase Reference)
[EPA Substance Registry System]

2-Propanamine, hydrochloride (15572-56-2)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RTECS ]

NT9530000
[TSCA ]

TSCA listed
[HS Code ]

2921199990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Carbamic acid, N-(diethoxyphosphinyl)-N-(1-methylethyl)-, 1,1-dimethylethyl ester-->TERT-BUTYLPHOSPHONIC DICHLORIDE-->Ramifenazone-->CYCLOHEXYLPHOSPHONIC DICHLORIDE-->tBuPO(NHiPr)2-->Isopropylamine-->Hydroxylamine hydrochloride-->Isobutyramide-->Ethanol
[Preparation Products]

Bentazone-->N,N-DIISOPROPYLBENZOTHIAZOLE-2-SULFENAMIDE-->endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol-->8-isopropyl-8-azabicyclo[3.2.1]octan-3-one-->N-Isopropylacetamide-->6-ISOPROPYL-5,6-DIHYDRO-1H-PYRROLO[3,4-D]PYRIMIDINE-2,4,7(3H)-TRIONE
Hazard InformationBack Directory
[Uses]

Isopropylamine Hydrochloride is an intermediate in the synthesis of 1-Cyano-3-isopropylguanidine (C955800).
[Synthesis]

Isopropylamine

75-31-0

ISOPROPYLAMINE HYDROCHLORIDE

15572-56-2

GENERAL PROCEDURE: Ammonium chloride (0.54 g, 10 mmol) and ethanol (3 mL) were added to a 25 mL round-bottom flask, followed by isopropylamine (10 mmol). The reaction mixture was placed on a magnetic stirrer and heated to reflux for 2 hours. After completion of the reaction, the solvent was removed by rotary evaporator to give propyl-2-amine hydrochloride as a solid in quantitative yield.

[References]

[1] Synthetic Communications, 2015, vol. 45, # 22, p. 2601 - 2607
Spectrum DetailBack Directory
[Spectrum Detail]

ISOPROPYLAMINE HYDROCHLORIDE(15572-56-2)MS
ISOPROPYLAMINE HYDROCHLORIDE(15572-56-2)1HNMR
ISOPROPYLAMINE HYDROCHLORIDE(15572-56-2)13CNMR
ISOPROPYLAMINE HYDROCHLORIDE(15572-56-2)IR1
ISOPROPYLAMINE HYDROCHLORIDE(15572-56-2)IR2
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

Isopropylamine Hydrochloride,>98.0%(T)(15572-56-2)
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