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Formic hydrazide - 90%, high purity , CAS No.624-84-0

    Grade & Purity:
  • ≥90%
In stock
Item Number
F109757
Grouped product items
SKU Size
Availability
Price Qty
F109757-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
F109757-10g
10g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$14.90
F109757-25g
25g
2
$28.90
F109757-100g
100g
2
$77.90
F109757-250g
250g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$175.90

Basic Description

Synonyms Formohydrazide; Formylhydrazide; Formylhydrazine; Monoformylhydrazine; N-Formylhydrazine; NSC 72391 | F11944 | V1D8X13QFN | XZBIXDPGRMLSTC-UHFFFAOYSA- | Formhydrazid | J-521389 | BCP26005 | 4-02-00-00085 (Beilstein Handbook Reference) | Formal hydrazine |
Specifications & Purity ≥90%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Formic hydrazide was used in the synthesis of 1,2,4-triazole derivatives. It was also used in the synthesis of new anticancer agent, 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(β-D-glucopyranosyl)-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazole-5,7(6H)-dione

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Class Carboxylic acids and derivatives
Subclass Carboxylic acid derivatives
Intermediate Tree Nodes Not available
Direct Parent Carboxylic acid hydrazides
Alternative Parents Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Carboxylic acid hydrazide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as carboxylic acid hydrazides. These are carboxylic acid derivatives containing a carbonyl group in which the carbon is directly linked to a hydrazide group (N-N).
External Descriptors Not available

Names and Identifiers

IUPAC Name formohydrazide
INCHI InChI=1S/CH4N2O/c2-3-1-4/h1H,2H2,(H,3,4)
InChIKey XZBIXDPGRMLSTC-UHFFFAOYSA-N
Smiles C(=O)NN
Isomeric SMILES C(=O)NN
WGK Germany 3
RTECS LQ8615000
Molecular Weight 60.06
Beilstein 635759
Reaxy-Rn 635759
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635759&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number Certificate Type Date Item
F2526351 Certificate of Analysis Jul 15, 2024 F109757
K1920219 Certificate of Analysis Sep 08, 2023 F109757
C2302555 Certificate of Analysis Jan 04, 2023 F109757
C2302556 Certificate of Analysis Jan 04, 2023 F109757
L2426210 Certificate of Analysis Jan 04, 2023 F109757
C2302831 Certificate of Analysis Jan 04, 2023 F109757
C2302554 Certificate of Analysis Jan 04, 2023 F109757
E1810047 Certificate of Analysis Mar 31, 2022 F109757

Chemical and Physical Properties

Solubility Soluble in water, ethanol and acetone.
Sensitivity heat & Moisture sensitive
Flash Point(°F) 233.6 °F
Flash Point(°C) 112℃
Boil Point(°C) 90 °C/0.7 mmHg
Melt Point(°C) 52-57°C
Molecular Weight 60.056 g/mol
XLogP3 -2.000
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 60.0324 Da
Monoisotopic Mass 60.0324 Da
Topological Polar Surface Area 55.100 Ų
Heavy Atom Count 4
Formal Charge 0
Complexity 20.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Jingyi Zhang, Zidan Cao, Di Fan, Yu Li, Tao Li, Baozeng Ren.  (2023)  Solid-liquid phase equilibrium of adiphenine hydrochloride in twelve pure solvents.  JOURNAL OF CHEMICAL THERMODYNAMICS,  183  (107067). 
2. Jianhang Qi, Jiale Liu, Yongming Ma, Yanjie Cheng, Kai Chen, Wenjing Hu, Junwei Xiang, Xiaoru Wang, Jianwei Zhao, Yang Zhou, Anyi Mei, Hongwei Han.  (2024)  Modulating Dual Functionalities of Hydrazide Derivatives for Iodide Oxidation Suppression and Defect Passivation in Printable Mesoscopic Perovskite Solar Cells.  Advanced Energy Materials,    (2402344). 

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