조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
NH2CONHNH2 · HCl
CAS 번호:
Molecular Weight:
111.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-247-0
Beilstein/REAXYS Number:
3593642
MDL number:
Assay:
≥99%
Quality Level
assay
≥99%
mp
175-177 °C (dec.) (lit.)
SMILES string
Cl.NNC(N)=O
InChI
1S/CH5N3O.ClH/c2-1(5)4-3;/h3H2,(H3,2,4,5);1H
InChI key
XHQYBDSXTDXSHY-UHFFFAOYSA-N
Application
Semicarbazide hydrochloride is a general reagent used to synthesize semicarbazones from aldehydes and ketones. It can be used to build a variety of heterocyclic compounds, some of which are potent antimicrobial and antiviral agents. It can also be used to prepare corrosion inhibitors.
Derivatization reagent for aldehydes and ketones which produces crystalline compounds with characteristic melting points.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 2 Oral
target_organs
Bone
저장 등급
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Synthesis and antimicrobial activity of some novel derivatives of benzofuran: Part 2. The synthesis and antimicrobial activity of some novel 1-(1-benzofuran-2-yl)-2-mesitylethanone derivatives.
Kirilmis C, et al.
European Journal of Medicinal Chemistry, 43(2), 300-308 (2008)
Semicarbazide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Experimental and theoretical evaluation of semicarbazones and thiosemicarbazones as organic corrosion inhibitors.
Goulart C M, et al.
Corrosion Science, 67, 281-291 (2013)


