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2615-84-1

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2615-84-1 Usage

Chemical structure

A long-chain alcohol compound with a hydroxyl group at the 2nd carbon and an amine group attached to the 1st carbon.

Common uses

Surfactant and emulsifier in cosmetic and personal care products (e.g., moisturizers, lotions, hair care products)
Ingredient in detergents, fabric softeners, and industrial cleaners

Functionality

Lowers surface tension and improves the solubility of ingredients
Exhibits antimicrobial properties
Provides conditioning effects

Benefits

Enhances the effectiveness of cleaning and personal care products

Versatility

Widely used in both consumer and industrial applications due to its multiple properties and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 2615-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2615-84:
(6*2)+(5*6)+(4*1)+(3*5)+(2*8)+(1*4)=81
81 % 10 = 1
So 2615-84-1 is a valid CAS Registry Number.

2615-84-1SDS

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 1-(2-hydroxyethylamino)dodecan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Dodecanol,1-[(2-hydroxyethyl)amino]

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:2615-84-1 SDS

2615-84-1Upstream product

2615-84-1Downstream Products

2615-84-1Relevant articles and documents

Synthesis and evaluation of antibacterial and antitumor activities of new galactopyranosylated amino alcohols

De Souza Fernandes, Fábio,Fernandes, Tayrine Silva,Da Silveira, Lígia Souza,Caneschi, Wiliam,Louren?o, Maria Cristina S.,Diniz, Claudio G.,De Oliveira, Pollyanna Francielli,Martins, Sabrina De Paula Lima,Pereira, Daiane Eleutério,Tavares, Denise Crispim,Le Hyaric, Mireille,De Almeida, Mauro V.,Couri, Mara Rubia C.

, p. 203 - 210 (2015/12/08)

Three series of d-galactose derivatives linked to a lipophilic aminoalcohol moiety were synthesized and their antibacterial activity was evaluated against Mycobacterium tuberculosis and representative species of Gram positive and Gram negative bacteria. Five out of the thirteen tested compounds displayed activity against M. tuberculosis, with a minimal inhibitory concentration (MIC) of 12.5 μg/mL and seven compounds were active against the four bacterial strains tested. The best results were obtained for amino alcohols 10 and 11 against Staphylococcus epidermidis (MIC Combining double low line 2 μg/mL). The antitumor activity was evaluated against three tumor cell lines (MCF-7, HeLa and MO59J) and compared to the normal cell line GM07492A. The results showed that the lowest IC50 values were observed for the amino alcohol 16 against MCF-7 (11.9 μM) and MO59J (10.0 μM).

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