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(1,1-Dimethylhexyl)amine, also known as DMHA, is an organic compound and a derivative of amphetamine. It is commonly used as a workout supplement and performance enhancer, classified as a stimulant that is believed to increase energy, focus, and alertness.
Used in Dietary Supplements Industry:
(1,1-Dimethylhexyl)amine is used as a workout supplement and performance enhancer for its stimulant properties, which are believed to increase energy, focus, and alertness.
Used in Pharmaceutical Industry:
(1,1-Dimethylhexyl)amine is used as a nasal decongestant, helping to relieve nasal congestion and improve breathing.
Used in Replacement for Banned Substances:
(1,1-Dimethylhexyl)amine has been marketed as a replacement for the banned substance DMAA in dietary supplements, offering an alternative for those seeking stimulant effects without the legal issues associated with DMAA.
Note: The use and regulation of (1,1-Dimethylhexyl)amine in dietary supplements is a topic of ongoing debate and research due to potential health risks and its similarity to other banned stimulants.

27581-29-9

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27581-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27581-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27581-29:
(7*2)+(6*7)+(5*5)+(4*8)+(3*1)+(2*2)+(1*9)=129
129 % 10 = 9
So 27581-29-9 is a valid CAS Registry Number.

27581-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethyl-hexylamine

1.2 Other means of identification

Product number -
Other names 2-amino-2-methylheptane

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:27581-29-9 SDS

27581-29-9Relevant academic research and scientific papers

Palladium-Catalyzed Arylation of Unactivated γ-Methylene C(sp3)-H and δ-C-H Bonds with an Oxazoline-Carboxylate Auxiliary

Ling, Peng-Xiang,Fang, Sheng-Long,Yin, Xue-Song,Chen, Kai,Sun, Bo-Zheng,Shi, Bing-Feng

, p. 17503 - 17507 (2016/01/25)

A palladium-catalyzed arylation of unactivated γ-methylene C(sp3)-H and remote δ-C-H bonds by using an oxazoline-carboxylate directing group has been developed. Arylation occurs with a broad substrate scope and high tolerance of functional groups (i.e., halogen, nitro, cyano, ether, trifluoromethyl, amine, and ester). The oxazoline-type auxiliary can be removed under acidic conditions.

HYDROXYETHYLAMINE DERIVATIVES FOR THE TREATMENT OF ALZHEIMER'S DISEASE

-

Page 77, (2010/02/07)

The present invention relates to novel hydroxyethylamine compounds of formula (I): (I) having Asp2 (-secretase, BACE1 or Memapsin) inhibitory activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases characterised by elevated-amyloid levels or-amyloid deposits, particularly Alzheimer's disease.

New approach to tertiary carbinamines

Gajda,Koziara,Napieraj,Sikora,Zwierzak

, p. 1385 - 1387 (2007/10/03)

Tertiary carbinamines (t-alkyl amines) can be conveniently obtained by dephosphorylation of diethyl N-t-alkylphosphoramidates 1 with 20% hydrochloric acid-tetrahydrofuran (1:1 v/v).

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