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128279

Sigma-Aldrich

Ethyl hydrazinoacetate hydrochloride

97%

Synonym(s):

(Carbethoxymethyl)hydrazine hydrochloride

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About This Item

Linear Formula:
H2NNHCH2CO2C2H5 · HCl
CAS Number:
6945-92-2
Molecular Weight:
154.60
Beilstein/REAXYS Number:
3912112
EC Number:
230-104-3
MDL number:
MFCD00012923
UNSPSC Code:
12352100
PubChem Substance ID:
24847839
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

assay

97%

form

powder

mp

152-154 °C (lit.)

functional group

amine
ester
hydrazine

SMILES string

Cl[H].CCOC(=O)CNN

InChI

1S/C4H10N2O2.ClH/c1-2-8-4(7)3-6-5;/h6H,2-3,5H2,1H3;1H

InChI key

HZZRIIPYFPIKHR-UHFFFAOYSA-N

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This Item
642436S220165875
Ethyl hydrazinoacetate hydrochloride 97%

128279

Ethyl hydrazinoacetate hydrochloride

2-Hydrazinobenzothiazole 97%

642436

2-Hydrazinobenzothiazole

Semicarbazide hydrochloride ≥99%

S2201

Semicarbazide hydrochloride

3-Methyl-2-benzothiazolinone hydrazone hydrochloride monohydrate ≥99.0% (HPLC)

65875

3-Methyl-2-benzothiazolinone hydrazone hydrochloride monohydrate

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

form

powder

form

solid

form

-

form

solid

mp

152-154 °C (lit.)

mp

198-202 °C (lit.)

mp

175-177 °C (dec.) (lit.)

mp

270-274 °C (dec.)

functional group

amine

functional group

hydrazine

functional group

-

functional group

thioether

Application

Ethyl hydrazinoacetate hydrochloride has been used in the preparation of three novel copper(II) complexes as condensation derivatives of 2-pyridinecarboxaldehyde, 2-acetylpyridine and 2-quinolinecarboxaldehyde[1].

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    STBG1506V
    S14667V
    S74273
    S14667
    12214CX

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    Nenad Filipović et al.
    Chemical biology & drug design, 84(3), 333-341 (2014-03-19)
    Novel Pd(II) complex with N-heteroaromatic Schiff base ligand, derived from 8-quinolinecarboxaldehyde (q8a) and ethyl hydrazinoacetate (haOEt), was synthesized and characterized by analytical and spectroscopy methods. The structure of novel complex, as well as structures of its quinoline and pyridine analogues
    Copper (II) complexes of N heteroaromatic hydrazones: Synthesis, X-ray structure, magnetic behavior, and antibacterial activity.
    Inorgorganica Chimica Acta, 362(6), 1996-2000 (2009)

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