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N-butyl-D-gluconamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 18375-57-0 Structure
  • Basic information

    1. Product Name: N-butyl-D-gluconamide
    2. Synonyms: N-butyl-D-gluconamide;Einecs 242-252-6
    3. CAS NO:18375-57-0
    4. Molecular Formula: C10H21NO6
    5. Molecular Weight: 251.27684
    6. EINECS: 242-252-6
    7. Product Categories: N/A
    8. Mol File: 18375-57-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 635.2°Cat760mmHg
    3. Flash Point: 337.9°C
    4. Appearance: /
    5. Density: 1.332g/cm3
    6. Vapor Pressure: 8.35E-19mmHg at 25°C
    7. Refractive Index: 1.543
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-butyl-D-gluconamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-butyl-D-gluconamide(18375-57-0)
    12. EPA Substance Registry System: N-butyl-D-gluconamide(18375-57-0)
  • 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: 18375-57-0(Hazardous Substances Data)

18375-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18375-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,7 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18375-57:
(7*1)+(6*8)+(5*3)+(4*7)+(3*5)+(2*5)+(1*7)=130
130 % 10 = 0
So 18375-57-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H21NO6/c1-2-3-4-11-10(17)9(16)8(15)7(14)6(13)5-12/h6-9,12-16H,2-5H2,1H3,(H,11,17)/t6-,7-,8+,9-/m1/s1

18375-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-D-gluconamide

1.2 Other means of identification

Product number -
Other names Einecs 242-252-6

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:18375-57-0 SDS

18375-57-0Downstream Products

18375-57-0Relevant articles and documents

Orthogonal construction of dual dynamic covalent linkages toward an “AND” logic-gate acid-/salt-responsive block copolymer

Nie, Wu-Cheng,Song, Fei,Xiao, Qian,Liu, Jiao-Jiao,Wang, Xiao-Hui,Zhou, Jiang-Ling,Chen, Si-Chong,Wang, Xiu-Li,Wang, Yu-Zhong

, p. 32 - 38 (2018)

A novel block copolymer is fabricated by orthogonally coupling two end-functionalized polymers, glucose-capped methoxypoly(ethylene glycol) (mPEG2k-diol) and phenylboronic acid-capped poly(ε-caprolactone) (PBA-PCL), with dual boronate ester and B–N/B–O dynamic covalent interactions. Due to their synergetic effect, this block copolymer can self-assemble into micelles in aqueous solution with high stability. More importantly, micellar disassembly can be only triggered in the presence of both signal inputs, acid and salt, displaying an “AND” logic-gate responsive behavior.

Synthesis and evaluation of D-gluconamides as green mineral scales

Reis, Marcelo I.P.,Gon?alves, Aline D.,Da Silva, Fernando De C.,Jord?o, Alessandro K.,Alves, Ricardo J.,De Andrade, Saulo Fernandes,Resende, Jackson A.L.C.,Rocha, Anderson A.,Ferreira, Vitor F.

experimental part, p. 6 - 12 (2012/07/02)

A series of 13 d-gluconamides were synthesized in moderate to good yields and evaluated as green scale inhibitors. The crystal structures of two compounds were determined by X-ray crystallography. The compounds 6c and 6d showed a reasonable inhibition of BaSO4 precipitation from aqueous solution (47% and 51%, respectively) that indicated the potential for these derivatives of δ-gluconolactone.

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