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Merck

55097

Glycine hydrochloride solution

100 mM amino acid in 0.1 M HCl, analytical standard

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C2H5NO2 · HCl
CAS 번호:
Molecular Weight:
111.53
NACRES:
NA.24
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
85151701
MDL number:
Beilstein/REAXYS Number:
3909617
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grade

analytical standard

Quality Level

assay

≥99.5%

form

liquid

analyte chemical class(es)

amino acids, peptides, proteins

concentration

100 mM amino acid in 0.1 M HCl

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

color

colorless

application(s)

food and beverages

format

single component solution

storage temp.

2-8°C

SMILES string

Cl.NCC(O)=O

InChI

1S/C2H5NO2.ClH/c3-1-2(4)5;/h1,3H2,(H,4,5);1H

InChI key

IVLXQGJVBGMLRR-UHFFFAOYSA-N

Application

Glycine hydrochloride in combination with 1-allyl-3-methylimidazolium chloride can find applications as an ionic liquid solvent, which can be used to dissolve chitosan and also fabricate chitosan/cellulose blend films with definite proportions of chitosan. It can also be used to treat the condition of achlorhydria.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.


pictograms

Corrosion

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2

flash_point_f

Not applicable

flash_point_c

Not applicable

저장 등급

12 - Non Combustible Liquids



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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문



Jr, M.J.J.
Encyclopedia of Chemical Processing and Design (1977)
Antibacterial blend films of cellulose and chitosan prepared from binary ionic liquid system
Fu R, et al.
Fibers and Polymers, 18, 852-858 (2017)
Emilie Macé et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 23(1), 7-16 (2014-08-07)
Most inherited retinal dystrophies display progressive photoreceptor cell degeneration leading to severe visual impairment. Optogenetic reactivation of retinal neurons mediated by adeno-associated virus (AAV) gene therapy has the potential to restore vision regardless of patient-specific mutations. The challenge for clinical