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292893

Sigma-Aldrich

Adipamide

98%

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About This Item

Linear Formula:
H2NCO(CH2)4CONH2
CAS Number:
628-94-4
Molecular Weight:
144.17
EC Number:
211-062-5
MDL number:
MFCD00008045
UNSPSC Code:
12352100
PubChem Substance ID:
24857616
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

226-229 °C (lit.)

solubility

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

functional group

amide

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

Application

Adipamide has been used in the preparation of bisimidates.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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.

JAN Code

292893-25G:
292893-5G:
292893-VAR:
292893-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8878
STBK7184
STBH7508
STBG6299
STBF7834V

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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
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.
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
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
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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