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CAS

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26153-91-3

(2,2-dimethylpropyl)methylamine(SALTDATA: HCl) is a chemical compound that features a tertiary amine group and is presented as a hydrochloride salt. This form allows it to crystallize, facilitating easier handling and storage. It is widely recognized for its role as a precursor in the synthesis of pharmaceuticals and other organic compounds, with its utility and properties being highly dependent on the specific application and context.

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  • 26153-91-3 Structure

  • Basic information

    1. Product Name: (2,2-dimethylpropyl)methylamine(SALTDATA: HCl)
    2. Synonyms: (2,2-dimethylpropyl)methylamine(SALTDATA: HCl);N,2,2-trimethylpropan-1-amine;1-Propanamine, N,2,2-trimethyl-
    3. CAS NO:26153-91-3
    4. Molecular Formula: C6H15N
    5. Molecular Weight: 101.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26153-91-3.mol

  • Chemical Properties

    1. Melting Point: -87.87°C (estimate)
    2. Boiling Point: 109.64°C (estimate)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.7400
    6. Refractive Index: 1.4000
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.76±0.30(Predicted)
    10. CAS DataBase Reference: (2,2-dimethylpropyl)methylamine(SALTDATA: HCl)(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2,2-dimethylpropyl)methylamine(SALTDATA: HCl)(26153-91-3)
    12. EPA Substance Registry System: (2,2-dimethylpropyl)methylamine(SALTDATA: HCl)(26153-91-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 26153-91-3(Hazardous Substances Data)

26153-91-3 Usage

Uses

Used in Pharmaceutical Synthesis:
(2,2-dimethylpropyl)methylamine(SALTDATA: HCl) serves as a crucial precursor in the creation of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Organic Compound Synthesis:
Beyond its pharmaceutical applications, (2,2-dimethylpropyl)methylamine(SALTDATA: HCl) is also utilized in the synthesis of a range of organic compounds. Its versatility in chemical reactions contributes to its importance in organic chemistry and related fields.
Used in Chemical Research:
In the realm of chemical research, (2,2-dimethylpropyl)methylamine(SALTDATA: HCl) is employed as a model compound to study the properties and reactions of tertiary amines, particularly in the context of hydrochloride salts and their behavior in different conditions.
Used in Industrial Chemical Production:
(2,2-dimethylpropyl)methylamine(SALTDATA: HCl) finds application in the industrial production of various chemicals, where its specific chemical characteristics are leveraged to produce desired outcomes in chemical processes and product development.

Check Digit Verification of cas no

The CAS Registry Mumber 26153-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,5 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26153-91:
(7*2)+(6*6)+(5*1)+(4*5)+(3*3)+(2*9)+(1*1)=103
103 % 10 = 3
So 26153-91-3 is a valid CAS Registry Number.

26153-91-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,2,2-trimethylpropan-1-amine

1.2 Other means of identification

Product number -
Other names N,2,2-trimethyl-1-propanamine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26153-91-3 SDS

26153-91-3Upstream product

26153-91-3Relevant articles and documents

Rate Increase in Consecutive Nucleophilic Aromatic Substitution Reactions of Trichlorotrinitrobenzene: The Synthesis of 1-(Alkylamino)-3,5-dichloro-2,4,6-trinitrobenzenes

Wolff, J. Jens,Zietsch, Andreas,Oeser, Thomas,Bolocan, Ion

, p. 5164 - 5168 (2007/10/03)

The title compounds are formed by the nucleophilic aromatic substitution reaction between symtrichlorotrinitrobenzene and amines. The yields and relative rates of formation depend critically on the degree of alkylation of the nucleophile. Contrary to the usual behavior, the introduction of a second and third donor is facilitated in the case of ammonia and monoalkylamines, while this is not the case for secondary amines. This behavior is rationalized on the basis of intramolecular hydrogen bonding and substantiated by an X-ray analysis of 3,5-dichloro-2,4,6-trinitroaniline.

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