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CAS

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2885-01-0

Butyl glycinate, also known as N-butylglycine, is a chemical compound with the molecular formula C6H13NO2. It is a derivative of glycine, an amino acid that serves as a building block for proteins in the human body. This versatile compound is valued for its moisturizing and conditioning properties, making it a common ingredient in cosmetic products, particularly in skincare.

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  • 2885-01-0 Structure

  • Basic information

    1. Product Name: butyl glycinate
    2. Synonyms: butyl glycinate;BUTYL 2-AMINOACETATE HCL
    3. CAS NO:2885-01-0
    4. Molecular Formula: C6H13NO2
    5. Molecular Weight: 131.17292
    6. EINECS: 220-745-7
    7. Product Categories: N/A
    8. Mol File: 2885-01-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: butyl glycinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: butyl glycinate(2885-01-0)
    11. EPA Substance Registry System: butyl glycinate(2885-01-0)

  • 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: 2885-01-0(Hazardous Substances Data)

2885-01-0 Usage

Uses

Used in Cosmetic Industry:
Butyl glycinate is used as a humectant in skincare products for its ability to retain moisture in the skin and hair, enhancing their hydration and conditioning effects.
Used in Pharmaceutical Industry:
Butyl glycinate is utilized in the production of pharmaceuticals and as a potential ingredient in the synthesis of new drugs, highlighting its importance in the development of novel medicinal compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2885-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2885-01:
(6*2)+(5*8)+(4*8)+(3*5)+(2*0)+(1*1)=100
100 % 10 = 0
So 2885-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-2-3-4-9-6(8)5-7/h2-5,7H2,1H3

2885-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 2-aminoacetate

1.2 Other means of identification

Product number -
Other names Butylaminoacetate

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:2885-01-0 SDS

2885-01-0Relevant articles and documents

A mild removal of Fmoc group using sodium azide

Chen, Chun-Chi,Rajagopal, Basker,Liu, Xuan Yu,Chen, Kuan Lin,Tyan, Yu-Chang,Lin, Fui,Lin, Po-Chiao

, p. 367 - 374 (2014/03/21)

A mild method for effectively removing the fluorenylmethoxycarbonyl (Fmoc) group using sodium azide was developed. Without base, sodium azide completely deprotected Nα-Fmoc-amino acids in hours. The solvent-dependent conditions were carefully studied and then optimized by screening different sodium azide amounts and reaction temperatures. A variety of Fmoc-protected amino acids containing residues masked with different protecting groups were efficiently and selectively deprotected by the optimized reaction. Finally, a biologically significant hexapeptide, angiotensin IV, was successfully synthesized by solid phase peptide synthesis using the developed sodium azide method for all Fmoc removals. The base-free condition provides a complement method for Fmoc deprotection in peptide chemistry and modern organic synthesis. Graphical Abstract: [Figure not available: see fulltext.]

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