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108-14-5

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108-14-5 Usage

General Description

2-chloropropyldimethylamine is an organic compound with the chemical formula C5H12ClN. It is a clear, colorless liquid with a strong ammonia-like odor. This chemical is widely used as an intermediate for the production of agricultural chemicals, dyes, and pharmaceuticals. It is also utilized as a corrosion inhibitor, emulsifying agent, and as a raw material for the synthesis of quaternary ammonium compounds. Additionally, 2-chloropropyldimethylamine is commonly employed in the synthesis of surfactants and as a chemical intermediate in the production of specialty chemicals. It is important to handle this chemical with care, as it is classified as a hazardous substance and can cause skin and eye irritation, as well as respiratory issues if inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 108-14-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108-14:
(5*1)+(4*0)+(3*8)+(2*1)+(1*4)=35
35 % 10 = 5
So 108-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H12ClN/c1-5(6)4-7(2)3/h5H,4H2,1-3H3

108-14-5SDS

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 2-chloro-N,N-dimethylpropan-1-amine

1.2 Other means of identification

Product number -
Other names Propylamine,2-chloro-N,N-dimethyl

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:108-14-5 SDS

108-14-5Relevant articles and documents

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Schultz,Sprague

, p. 50 (1948)

-

-

Amundsen,Pitts

, p. 1494,1497 (1951)

-

COMPOSITIONS AND METHODS FOR THE TREATMENT OF SEVERE PAIN

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, (2013/12/03)

The invention relates to the compounds of formula (I) or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compounds of formula (I), and methods for the treatment of severe pain may be formulated for oral, buccal, rectal, topical, transdermal, transmucosal, intravenous, parenteral administration, syrup, or injection. Such compositions may be used to treatment of chronic pain, generalized pain disorders, leukemia, cancer, chronic pain, chemotherapy induced pain, epilepsy, migraine, neuropathic pain, post herpetic neuralgia, neuralgia, pain, drug addiction, detoxification of drugs, Alzheimer's disease, multiple sclerosis, multiple sclerosis restless legs syndrome (RLS), cluster headache, depression, fibromyalgia, amyotrophic lateral sclerosis (ALS), convulsions, partial seizures, mood-stabilizing agent and bipolar disorder.

PHENOTHIAZINE DERIVATIVES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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, (2008/06/13)

Phenothiazine derivatives of formula: STR1 in which Y is hydrogen or halogen, R 1 and R 2, which may be identical or different, denote alkyl, cycloalkyl-alkyl, hydroxyalkyl or acetyloxyalkyl radicals or form, together with the nitrogen atom to which they are attached, an optionally substituted, saturated or partially unsaturated 4-to 7-membered heterocycle; and either X is oxygen, sulphur or: N-R 4, R is cycloalkyl, phenyl or--CH 2 R 3, R 3 is H, alkyl (1 to 5 C), alkenyl or alkynyl (2 to 4 C), cycloalkyl (3 to 6 C), phenyl, substituted phenyl or a heterocyclic radical, R 4 is H or--CN, except that X is not oxygen if, simultaneously, R 3 is H or alkyl, R. sub.1 and R 2 are alkyl or NR 1 R 2 forms an unsubstituted heterocycle, and Y is H; or X is: N-R 4 and R 4 forms, with R and the neighbouring atoms, an optionally substituted imidazolyl or imidazolinyl radical or a hexahydrobenzimidazolyl radical, in their isomeric forms and mixtures thereof and their acid addition salts are useful as analgesics and diuretics.

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