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Safety Information

292893

Sigma-Aldrich

Adipamide

98%

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Linear Formula:
H2NCO(CH2)4CONH2
CAS Number:
Molecular Weight:
144.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

mp

226-229 °C (lit.)

solubility

formic acid: soluble 50 mg/mL, clear, colorless to faintly yellow

SMILES string

NC(=O)CCCCC(N)=O

InChI

1S/C6H12N2O2/c7-5(9)3-1-2-4-6(8)10/h1-4H2,(H2,7,9)(H2,8,10)

InChI key

GVNWZKBFMFUVNX-UHFFFAOYSA-N

Related Categories

Application

Adipamide has been used in the preparation of bisimidates.

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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S J Kennel et al.
Toxicology and applied pharmacology, 82(2), 256-263 (1986-02-01)
A thyroglobulin conjugate of dioxin (thyroglobulin-2 adipamide, 3,7,8-trichlorodibenzo-p-dioxin) (TG-TCDD) was used to immunize BALB/c mice. Hybridomas were produced by cell fusion between immune spleen cells and mouse myelomas SP2/0, P3, or NS1. To screen the thousands of resultant cultures for
Xuejiang Wang et al.
Biomaterials, 23(24), 4787-4791 (2002-10-04)
In this study, acicular nano-hydroxyapatite (n-HA) was used to make a new biomimetic composite with polyamide (poly hexamethylene adipamide) by a unique technique. The physical and chemical characteristics of the composites were tested. It was found that these synthesized n-HA
D L Morris et al.
The Biochemical journal, 147(3), 593-603 (1975-06-01)
Triethyloxonium tetrafluoroborate was used to O-alkylate nylon-tube thus producing the imidate salt of the nylon which was further made to react with 1,6-diaminohexane. 2. Hexokinase (EC 2.7.1.1) and glucose 6-phosphate dehydrogenase (EC 1.1.1.49) were immobilized on the amino-substituted nylon tube
Colin C Seaton et al.
Chemical communications (Cambridge, England), (8)(8), 880-881 (2002-07-19)
The crystal structure of a previously unknown triclinic polymorph of adipamide has been solved from laboratory X-ray powder diffraction data using a new direct space global optimisation method based on differential evolution.
R W Fleischman et al.
Journal of environmental pathology and toxicology, 3(5-6), 149-170 (1980-06-01)
As a part of the National Cancer Institute's effort to screen environmental and occupational chemicals for chronic toxicity and carcinogenicity, the amides acetamide, hexanamide, adipamide, urea, and p-tolylurea were fed to male and female C57B1/6 mice and Fischer 344 rats

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