121150-43-4

• 

• Basic information

  1. Product Name: dodecyl-N,N-dimethylaminoacetate
  2. Synonyms: dodecyl-N,N-dimethylaminoacetate;N,N-Dimethylglycine dodecyl ester
  3. CAS NO:121150-43-4
  4. Molecular Formula: C16H33NO2
  5. Molecular Weight: 271.44
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 121150-43-4.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 336.6°Cat760mmHg
  3. Flash Point: 93.7°C
  4. Appearance: /
  5. Density: 0.894g/cm³
  6. Vapor Pressure: 0.000111mmHg at 25°C
  7. Refractive Index: 1.45
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: dodecyl-N,N-dimethylaminoacetate(CAS DataBase Reference)
  11. NIST Chemistry Reference: dodecyl-N,N-dimethylaminoacetate(121150-43-4)
  12. EPA Substance Registry System: dodecyl-N,N-dimethylaminoacetate(121150-43-4)

• 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: 121150-43-4(Hazardous Substances Data)

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• Downstream Products
• Article

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• Glycine, N,N-dimethyl-,dodecyl ester

  Cas No: 121150-43-4

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• dodecyl-N,N-dimethylaminoacetate

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121150-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121150-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,5 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121150-43:
(8*1)+(7*2)+(6*1)+(5*1)+(4*5)+(3*0)+(2*4)+(1*3)=64
64 % 10 = 4
So 121150-43-4 is a valid CAS Registry Number.

InChI:InChI=1/C16H33NO2/c1-4-5-6-7-8-9-10-11-12-13-14-19-16(18)15-17(2)3/h4-15H2,1-3H3

121150-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-(dimethylamino)tetradecanoate

1.2 Other means of identification

Product number	-
Other names	N,N-Dimethylglycine dodecyl ester

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:121150-43-4 SDS

121150-43-4Upstream product

• 6316-04-7 dodecyl 2-chloroacetate 
• 1118-68-9 dimethylaminoacetic acid 
• 112-53-8 1-dodecyl alcohol 
• 50-00-0 formaldehyd 
• 13827-65-1 dodecyl 2-aminoacetate 
• 2491-06-7 N,N-dimethylglycine hydrochoride 

121150-43-4Downstream Products

121150-43-4Relevant articles and documents

Unusual rate enhancement of bimolecular dehydrocondensation to form amides at the interface of micelles of fatty acid salts

Kunishima, Munetaka,Imada, Hiroko,Kikuchi, Kanako,Hioki, Kazuhito,Nishida, Jin,Tani, Shohei

, p. 7254 - 7257 (2005)

(Chemical Equation Presented) Speeding up: A micelle-water interface acts as a suitable reaction field for dehydrocondensation. The coupling reaction of fatty acid salts with a triazine-type amphiphilic dehydrocondensing agent in a micellar system (see picture) underwent up to 2000-fold acceleration. The rate enhancement can be attributed to the higher local concentration and preorientation of the reactants in the micelles.

Method of inducing a phase transition of a bilayer membrane vesicle

-

Page/Page column 16; 17, (2018/11/10)

Provided is a bilayer membrane vesicle capable of undergoing a phase transition. The bilayer membrane vesicle includes: (a) a fatty acid salt having 6 to 20 carbon atoms; (b) an alcohol or an amine compound having an aliphatic chain of 6 to 20 carbon atoms; and (c) an artificial synthetic lipid or a phospholipid capable of forming a bilayer membrane. Preferably, this bilayer membrane vesicle further contains (d) a tertiary amine as a component of the membrane. Also provided is a method of inducing a phase transition of a bilayer membrane vesicle, the method including the step of adding a dehydrating condensing agent or a dehydrating condensing agent precursor having the property of accumulating at an interface to the bilayer membrane vesicle. By causing the lipids that form a molecular aggregate to chemically change, it is possible to change the physical property and the morphology of the molecular aggregate and control the timing of phase transitions such as membrane fusion. In the membrane fusion, for example, fusion can occur without leakage of the contents of the bilayer membrane vesicle.

ANTIMICROBIAL COMPOUNDS AND METHODS OF USE

-

Paragraph 0237; 0239, (2014/06/25)

The present disclosure provides antimicrobial compounds, compositions comprising such antimicrobial compounds, and methods of their use, in particular, antibacterial compounds and antifungal compounds. In certain aspects, the antimicrobial compounds are e

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