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Merck

33226

Sigma-Aldrich

Glicina

puriss. p.a., reag. Ph. Eur., buffer substance, 99.7-101% (calc. to the dried substance)

Sinónimos:

Glicocola, Ácido aminoacético, Ácido aminoetanoico

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About This Item

Fórmula lineal:
NH2CH2COOH
Número de CAS:
Peso molecular:
75.07
Beilstein/REAXYS Number:
635782
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.21

agency

USP/NF
reag. Ph. Eur.

Quality Level

grade

puriss. p.a.

assay

99.7-101% (calc. to the dried substance)

form

crystalline powder

technique(s)

IR spectroscopy: suitable

impurities

≤0.001% heavy metals (as Pb)
≤0.02% ammonium (NH4)
≤0.1% water (Karl Fischer)
≤1.0% ninhydrin-positive substances

ign. residue

≤0.05% (as SO4)

loss

≤0.5% loss on drying, 105°C, 2 h

pH

5.9-6.4 (20 °C, 5%)

pKa (25 °C)

(1) 2.35, (2) 9.60
2.35

mp

240 °C (dec.) (lit.)

anion traces

chloride (Cl-): ≤30 mg/kg
sulfate (SO42-): ≤20 mg/kg

cation traces

Fe: ≤5 mg/kg

suitability

in accordance for identity (IR)

SMILES string

NCC(O)=O

InChI

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

InChI key

DHMQDGOQFOQNFH-UHFFFAOYSA-N

Gene Information

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Application

Glycine can be used as:
  • A reactant in the natural soil clay-catalyzed cleavage and polycondensation with pyrogallol.
  • A catalyst in the Knoevenagel reaction between aryl aldehydes and malononitrile to form a C=C bond.
  • A reagent in the metal-free synthesis of biaryls from aryl sulfoxides and sulfonanilides via sigmatropic rearrangement.

Biochem/physiol Actions

Neurotransmisor inhibidor de la médula espinal, regulador alostérico de los receptores NMDA.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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