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686166

Sigma-Aldrich

2-Amino-5-methyl-1,3,4-thiadiazole

97%

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About This Item

Empirical Formula (Hill Notation):
C3H5N3S
CAS Number:
108-33-8
Molecular Weight:
115.16
EC Number:
203-573-7
MDL number:
MFCD00003110
UNSPSC Code:
12352100
PubChem Substance ID:
329761026
NACRES:
NA.22

Assay

97%

form

solid

mp

223-228 °C

SMILES string

Cc1nnc(N)s1

InChI

1S/C3H5N3S/c1-2-5-6-3(4)7-2/h1H3,(H2,4,6)

InChI key

HMPUHXCGUHDVBI-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Jingjing Zhang et al.
Carbohydrate polymers, 215, 108-118 (2019-04-15)
In the current study, five novel urea-functionalized chitosan derivatives were synthesized via condensation reactions of chloroacetyl chitosan (CTCS) with urea groups bearing nitrogen-containing heterocycles. In order to identify the structure characteristics of chitosan derivatives, FT-IR, 1H NMR spectroscopy, and elemental
Jingjing Zhang et al.
Carbohydrate polymers, 234, 115903-115903 (2020-02-20)
In this study, 2-urea-chitosan oligosaccharide derivatives (2-urea-COS derivatives) and 2,6-diurea-chitosan oligosaccharide derivatives (2,6-diurea-COS derivatives) were successfully designed and synthesized via intermediate 2-methoxyformylated chitosan oligosaccharide. All samples were characterized and compared based on FT-IR, 1H NMR spectroscopy, and elemental analysis. The

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