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259748

Hydrazine acetate

97%

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About This Item

Linear Formula:
H2NNH2 · CH3CO2H
CAS Number:
7335-65-1
Molecular Weight:
92.10
NACRES:
NA.22
PubChem Substance ID:
24855432
UNSPSC Code:
12352100
EC Number:
230-845-2
MDL number:
MFCD00013141
Assay:
97%
Form:
crystals
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Quality Level

200

assay

97%

form

crystals

mp

100-102 °C (lit.)

functional group

carboxylic acid, hydrazine

SMILES string

NN.CC(O)=O

InChI

1S/C2H4O2.H4N2/c1-2(3)4;1-2/h1H3,(H,3,4);1-2H2

InChI key

YFHNDHXQDJQEEE-UHFFFAOYSA-N

General description

Hydrazine acetate is an acetate salt of hydrazine. It is used as a reagent for the cleavage of glycosidic esters and anomeric denitration of carbohydrates. In organic synthesis, it is also used as a building block to prepare various organic derivatives.

Application

Hydrazine acetate has been used in preparation of:
  • 2,3,5-tri-O-acetyl-α-L-arabinofuranosyl trichloroacetimidate
  • disaccharide 4-methoxyphenyl glycoside

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

7335-65-1

CAS No.

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Certificates of Analysis (COA)

Lot/Batch Number
01329DJ
13115KH
01407BH
01726LE
01224EE

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S Deng et al.
Carbohydrate research, 317(1-4), 53-62 (1999-08-31)
Dioscin, polyphyllin D, and balanitin 7, which belong to a group of structurally similar diosgenyl saponins with promising bioactivities, were synthesized by stepwise glycosylation.
T M Slaghek et al.
Carbohydrate research, 255, 61-85 (1994-03-04)
The synthesis is reported of 4-methoxyphenyl O-(beta-D-glucopyranosyluronic acid)-(1-->3)-2-acetamido-2-deoxy-beta-D-glucopyranoside (1), 4-methoxyphenyl O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1-->4)-O-(beta-D- glucopyranosyluronic acid)-(1-->3)-2-acetamido-2-deoxy-beta-D-glucopyranoside (5), and 4-methoxyphenyl O-(beta-D-glucopyranosyluronic acid)-(1-->3)-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-(1-->4)-O-(b eta-D- glucopyranosyluronic acid)-(1-->3)-2-acetamido-2-deoxy-beta-D-glucopyranoside (10), which are structural elements of the extracellular polysaccharide hyaluronic acid. 6-O-Levulinoyl-2,3,4-tri-O-p-toluoyl-alpha-D-glucopyranosyl trichloroacetimidate (3) was condensed with 4-methoxyphenyl 2-deoxy-4,6-O-isopropylidene-2-phthalimido-beta-D-glucopyranoside

Global Trade Item Number

SKUGTIN
259748-25G04061832099125
259748-5G04061826075432