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Assay
99%
form
powder
optical activity
[α]25/D +21°, c = 2 in ethanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
90-92 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cl[H].CCOC(=O)[C@@H](N)CCSC
InChI
1S/C7H15NO2S.ClH/c1-3-10-7(9)6(8)4-5-11-2;/h6H,3-5,8H2,1-2H3;1H/t6-;/m0./s1
InChI key
KPWCQEUBJAIORR-RGMNGODLSA-N
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Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Studies on methionine derivatives as possible sources of protected methionine in ruminant rations.
Journal of the science of food and agriculture, 33(10), 949-956 (1982-10-01)
Journal of hazardous materials, 350, 169-179 (2018-02-27)
Cyclopolymerization of N,N-diallylmethionine hydrochloride, derived from the biogenic amino acid methionine, (90 mol%) and cross-linker tetraallylpiperazinium dichloride (10 mol%) in presence of an azo-initiator afforded pH-responsive cross-linked polyzwitterion (CPZ). The structural morphology of the resin (i.e. CPZ) was examined by the BET
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