DEF0017503MA - - Google Patents

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Publication number

DEF0017503MA

DEF0017503MA DEF0017503MA DE F0017503M A DEF0017503M A DE F0017503MA DE F0017503M A DEF0017503M A DE F0017503MA

Authority

DE

Germany

Prior art keywords

salts

sarcosine anhydride

pas

sarcosine

ecm

Prior art date

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

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• 150000003839 salts Chemical class 0.000 claims description 9
• GPAYXCOQADGNAZ-UHFFFAOYSA-N [2-(methylamino)acetyl] 2-(methylamino)acetate Chemical compound CNCC(=O)OC(=O)CNC GPAYXCOQADGNAZ-UHFFFAOYSA-N 0.000 claims description 8
• 239000007864 aqueous solution Substances 0.000 claims description 6
• WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical class NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 claims description 2
• -1 Salts sarcosine anhydride Chemical class 0.000 claims description 2
• 239000000203 mixture Substances 0.000 claims description 2
• 230000000087 stabilizing effect Effects 0.000 claims description 2
• YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 1
• 239000003381 stabilizer Substances 0.000 claims 1
• CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 8
• 229940018563 3-aminophenol Drugs 0.000 description 4
• 239000002253 acid Substances 0.000 description 3
• 239000000243 solution Substances 0.000 description 3
• CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
• 239000003638 chemical reducing agent Substances 0.000 description 2
• 238000000354 decomposition reaction Methods 0.000 description 2
• WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
• 230000003647 oxidation Effects 0.000 description 2
• 238000007254 oxidation reaction Methods 0.000 description 2
• TUDXHDSCPJSDIO-UHFFFAOYSA-N 4-amino-2-hydroxybenzoic acid;sodium Chemical compound [Na].NC1=CC=C(C(O)=O)C(O)=C1 TUDXHDSCPJSDIO-UHFFFAOYSA-N 0.000 description 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
• FSYKKLYZXJSNPZ-UHFFFAOYSA-N N-methylaminoacetic acid Natural products C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
• 108010077895 Sarcosine Proteins 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 239000001569 carbon dioxide Substances 0.000 description 1
• 229910002092 carbon dioxide Inorganic materials 0.000 description 1
• 238000006114 decarboxylation reaction Methods 0.000 description 1
• 238000002845 discoloration Methods 0.000 description 1
• 150000007530 organic bases Chemical class 0.000 description 1
• 108090000623 proteins and genes Proteins 0.000 description 1
• 229940043230 sarcosine Drugs 0.000 description 1
• 229910052708 sodium Inorganic materials 0.000 description 1
• 239000011734 sodium Substances 0.000 description 1
• VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
• 159000000000 sodium salts Chemical class 0.000 description 1
• 230000006641 stabilisation Effects 0.000 description 1
• 238000011105 stabilization Methods 0.000 description 1
• 239000008174 sterile solution Substances 0.000 description 1
• 231100000331 toxic Toxicity 0.000 description 1
• 230000002588 toxic effect Effects 0.000 description 1
• 231100000419 toxicity Toxicity 0.000 description 1
• 230000001988 toxicity Effects 0.000 description 1
• 201000008827 tuberculosis Diseases 0.000 description 1